Clamp, Vascular, Reprocessed
FDA product code NMF · 3 cleared devices
Class 2
Cardiovascular
- Regulation
- 21 CFR 870.4450
- Review panel
- CV
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 2001-12-21 – 2012-04-03
Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).
NMF
2012-04-03
NMF
2002-07-18
REPROCESSED FEMORAL COMPRESSION DEVICE
View details →
NMF
2001-12-21
VANGUARD REPROCESSED FEMORAL COMPRESSION DEVICE
View details →No matching devices.
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