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Interlace Medical Inc. Premarket Notification 5.
- https://www.accessdata.fda.gov/cdrh_docs/pdf10/K100559.pdf
- Interlace Medical Inc. Premarket Notification 5. 510(k) SUMMARY ~if 1. Submitter: Interlace Medical Inc. lIR~0 135 Newbury St Framingham, MA 0 1701 Telephone: …
510(k) Premarket Notification
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=k073690
- FOIA Releasable 510(k) K073690: Device Name: INTERLACE MEDICAL HYSTEROSCOPIC MORCELLATION SYSTEM: Applicant: INTERLACE MEDICAL, INC. …
510(k) Premarket Notification
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=27655
- FOIA Releasable 510(k) K081070: Device Name: INTERLACE MEDICAL OPERATIVE HYSTEROSCOPY SYSTEM: Applicant: INTERLACE MEDICAL, INC. 139 NEWBURY …
510(k) Premarket Notification - Food and Drug …
- https://www.accessdata.fda.gov/scrIpts/cdrh/cfdocs/cfpmn/pmn.cfm?id=K091100
- Date Received: 04/16/2009: Decision Date: 10/23/2009: Decision: Substantially Equivalent (SESE) Regulation Medical Specialty: Obstetrics/Gynecology 510k Review Panel
510(k) Premarket Notification
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=k100559
- 510(k) Number: K100559: FOIA Releasable 510(k) K100559: Device Name: MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM: Applicant: INTERLACE MEDICAL …
510(k) SUMMARY OCT 2 3 2009 - Food and Drug …
- https://www.accessdata.fda.gov/cdrh_docs/pdf9/K091100.pdf
- Interlace Medical Inc. Premarket Notification 5. 510(k) SUMMARY OCT 2 3 2009 1. Submitter: Interlace Medical Inc. 135 Newbury St Framingham, MA 01701 …
Interlace Medical Inc. Ac~~~~~~~~~ P5 f - Food and …
- https://www.accessdata.fda.gov/cdrh_docs/pdf10/K102686.pdf
- Interlace Medical Inc. Ac~~~~~ Premarket Notification frtfO P5 2o "f 8 5. 510(k) SUMMARYOC 1520 1. Submitter: Interlace Medical Inc. 135 Newbury St Framingham, …
Interlace Medical APR 1 7 ZOOB - Food and Drug …
- https://www.accessdata.fda.gov/cdrh_docs/pdf7/K073690.pdf
- 510(k) Number (if known): K073690 Device Name: Interlace Medical Hysteroscopic Morcellation System Indications For Use: The Interlace Medical Hysteroscopic …
Search the Releasable 510(k) Database | FDA
- https://www.fda.gov/medical-devices/510k-clearances/search-releasable-510k-database
- You can search the releasable 510(k) database by Panel, 510(k) number, Product code or Device name. A search query will produce information from the database in the following …
510(k) Clearances | FDA - U.S. Food and Drug …
- https://www.fda.gov/medical-devices/device-approvals-denials-and-clearances/510k-clearances
- Overview. Section 510 (k) of the Food, Drug and Cosmetic Act requires device manufacturers who must register, to notify FDA of their intent to market a medical …
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