Medical Device Prescription Requirements

Overview of Regulatory Requirements: Medical Devices

https://www.fda.gov/training-and-continuing-education/cdrh-learn/overview-regulatory-requirements-medical-devices-transcript

This module is intended to provide an overview of the regulatory requirements for medical devices or what is sometimes referred to as Devices 101. The US Food and Drug Administration (FDA) is ...

Durable Medical Equipment, Prosthetics, Orthotics and …

https://www.cms.gov/Research-Statistics-Data-and-Systems/Monitoring-Programs/Medicare-FFS-Compliance-Programs/Medical-Review/FacetoFaceEncounterRequirementforCertainDurableMedicalEquipment

Over-the-Counter (OTC) Medical Devices: …

https://www.fda.gov/medical-devices/products-and-medical-procedures/over-counter-otc-medical-devices-considerations-device-manufacturers

Over-the-counter (OTC) medical devices are those that may be offered for sale directly to the consumer. In other words, these devices do not require a …

Device Labeling | FDA - U.S. Food and Drug Administration

https://www.fda.gov/medical-devices/overview-device-regulation/device-labeling

Device Advice - Introduction to labeling requirements for medical devices, including advertising, over the counter, exemptions, in vitro diagnostics, investigational …

Medical Devices | FDA - U.S. Food and Drug Administration

https://www.fda.gov/Medical-Devices

CDRH 2022 Annual Report. Accomplishments for 2022, including the Pandemic Response, MDUFA V, Device Innovation, over-the-counter (OTC) hearing aid final rule, and device …

CFR - Code of Federal Regulations Title 21 - Food and …

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfCFR/CFRSearch.cfm?fr=801.109

The information on this page is current as of Nov 29, 2022. For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR). …

Importing Medical Devices | FDA

https://www.fda.gov/industry/importing-fda-regulated-products/importing-medical-devices

Importing FDA medical device. Medical device classification, pre-market submission, medical device registration and listing, 510(k), PMA, medical device labeling

How to Determine if Your Product is a Medical Device | FDA

https://www.fda.gov/medical-devices/classify-your-medical-device/how-determine-if-your-product-medical-device

The following steps may be helpful when trying to determine if a product is regulated by the FDA as a medical device. Step 1: Determine if your product meets the …

801.109 - Prescription devices. - LII / Legal Information …

https://www.law.cornell.edu/cfr/text/21/801.109

A device which, because of any potentiality for harmful effect, or the method of its use, or the collateral measures necessary to its use is not safe except under the supervision of a …

Class I and Class II Device Exemptions | FDA

https://www.fda.gov/medical-devices/classify-your-medical-device/class-i-and-class-ii-device-exemptions

Most class I and some class II devices are exempt from 510 (k) requirements, subject to certain limitations (see section 510 (l) (1) of the Federal Food, …