NMF · Class II · 21 CFR 870.4450

FDA Product Code NMF: Clamp, Vascular, Reprocessed

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).

Leading manufacturers include Sterilmed, Inc. and Vanguard Medical Concepts, Inc..

3
Total
3
Cleared
202d
Avg days
2001
Since

FDA 510(k) Cleared Clamp, Vascular, Reprocessed Devices (Product Code NMF)

3 devices
1–3 of 3
Cleared Apr 03, 2012
REPROCESSED FEMORAL COMPRESSION DEVICE
K120204
Sterilmed, Inc.
Cardiovascular · 71d
Cleared Jul 18, 2002
REPROCESSED FEMORAL COMPRESSION DEVICE
K012574
Sterilmed, Inc.
Cardiovascular · 343d
Cleared Dec 21, 2001
VANGUARD REPROCESSED FEMORAL COMPRESSION DEVICE
K011832
Vanguard Medical Concepts, Inc.
Cardiovascular · 192d

About Product Code NMF - Regulatory Context