NMFClass II

Clamp, Vascular, Reprocessed

21 CFR 870.4450 / Cardiovascular

NMF is the FDA product code for Clamp, Vascular, Reprocessed, a class II device type, regulated under 21 CFR 870.4450. FDA's definition for this code reads: "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)". As of 2026-09-10, FDA records hold 3 510(k) clearances under this code, the most recent dated 2012-04-03, and 2 recalls.

Classification record

Product code: NMF
Device name: Clamp, Vascular, Reprocessed
FDA definition: 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).
Regulation: 21 CFR 870.4450
Device class: Class II
Review panel: Cardiovascular
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 3
Ingested recalls: 2

Clearances, product code NMF

By decision year

3 clearances under product code NMF with a decision year between 2001 and 2012, 2001 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code NMF by decision year
Year	Clearances
2001	1
2002	1
2012	1

Applicants with the most clearances

Product code NMF

Applicants holding the most 510(k) clearances under product code NMF
Applicant	Clearances
Sterilmed Inc	2
Stryker Sustainability Solutions	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code NMF.