NMF — Clamp, Vascular, Reprocessed Class II

FDA Device Classification

Classification Details

Product Code: NMF
Device Class: Class II
Regulation Number: 870.4450
Submission Type
Review Panel: CV
Medical Specialty: Cardiovascular
Implant: No

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).

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K120204	sterilmed	REPROCESSED FEMORAL COMPRESSION DEVICE	April 3, 2012
K012574	sterilmed	REPROCESSED FEMORAL COMPRESSION DEVICE	July 18, 2002
K011832	vanguard medical concepts	VANGUARD REPROCESSED FEMORAL COMPRESSION DEVICE	December 21, 2001