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Product codes
NMF
Product code NMF
Device name
Clamp, Vascular, Reprocessed
Medical specialty
Cardiovascular
Device class
2
Regulation number
870.4450
Review panel
CV
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
Y
Summary malfunction reporting
Ineligible
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).
Source
FDA openFDA device classification dataset
Related 510(k) Records
#
510(k), Device, Applicant table
510(k)
Device
Applicant
Decision date
K120204
REPROCESSED FEMORAL COMPRESSION DEVICE
Sterilmed, Inc.
2012-04-03
K012574
REPROCESSED FEMORAL COMPRESSION DEVICE
Sterilmed, Inc.
2002-07-18
K011832
VANGUARD REPROCESSED FEMORAL COMPRESSION DEVICE
Vanguard Medical Concepts, Inc.
2001-12-21
Related GUDID Devices
#
Primary DI, Brand, Company table
Primary DI
Brand
Company
Published
10888551034814
NA
STERILMED, INC.
2016-09-22
10888551039482
NA
STERILMED, INC.
2016-09-22