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Biosphere Medical : BioSphere Medical Receives FDA …
- https://www.marketscreener.com/quote/stock/BIOSPHERE-MEDICAL-INC-8626/news/Biosphere-Medical-BioSphere-Medical-Receives-FDA-Approval-For-QuadraSphere-TM-Microspheres-250178/
- BioSphere Medical, Inc. , a medical device company that pioneered the use of bioengineered microspheres to treat uterine fibroids, hypervascularized tumors and ... | …
510(k) Premarket Notification
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K021397
- 510 (k) Number. K021397. Device Name. EMBOSPHERE MICROSPHERES AND EMBOGOLD MICROSPHERES FOR USE IN UTERINE FIBROID EMBOLIZATION. …
Embosphere® Microspheres - Consistent …
- https://www.merit.com/peripheral-intervention/embolotherapy/microspheres/embosphere-microspheres/
- Embosphere Microspheres, the most clinically studied round embolic, provide consistent and predictable results for …
Biosphere Medical – THE RIGHT CHOICE IS RIGHT HERE
- https://www.biosphere-medical.com/
- Biosphere Medical offers healthcare equipment and services from world leaders in the medical sector. Complete coverage for biomedical equipment such as Life Support …
Bioness L300 Go
- https://www.l300go.com/hcp/
- Individual results may vary. Consult with a qualified physician to determine if these products are right for you. Important Safety Information and Risks: For Indications for Use, …
Our Products – Biosphere Medical
- https://www.biosphere-medical.com/products/
- Biosphere Medical offers medical consumables for day to day use. We take care of most of the daily requirements of the hospitals such as syringes, dressings, gloves and all such …
510(k) Summary for the BioSphere Medical, Inc.
- https://www.accessdata.fda.gov/cdrh_docs/pdf5/K052742.pdf
- for the BioSphere Medical, Inc. QuadraSphereTM Microspheres 1. SUBMITTERI510(K) HOLDER BioSphere Medical, Inc. 1050 Hingham Street Rockland, …
BioSphere Medical QuadraSphere® Microspheres …
- https://www.accessdata.fda.gov/cdrh_docs/pdf11/K113822.pdf
- BioSphere Medical QuadraSphere® Microspheres 30 to 6Opm <II3 Special 510O(k): Device Modification Notification MAR -82012 510(K) SUMMARY Submitter Name: …
Biosphere Medical, S.A. Alix Fonlladosa
- https://www.accessdata.fda.gov/cdrh_docs/pdf18/K183578.pdf
- Biosphere Medical, S.A. Alix Fonlladosa Regulatory Affairs Manager Parc des Nations – Paris Nord 2, 383 rue de la Belle Etoile Roissy en France, 95700 Fr Re: K183578 ... 801); …
510(k) Premarket Notification
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K052742
- Date Received: 09/30/2005: Decision Date: 11/07/2006: Decision: Substantially Equivalent (SESE) Regulation Medical Specialty: Cardiovascular 510k Review Panel
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