FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ULNAR-RADIAL APPROXIMATER

K Number: K780291 · Decision Feb 28, 1978
Classifications
1
FEI Numbers
274
Registration Numbers
274
Same Product Code
31
Applicant Total
140
Review Days
7

Basic Information

Device Name
ULNAR-RADIAL APPROXIMATER
K Number
K780291
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
EDWARD WECK, INC.
Date Received
February 21, 1978
Decision Date
February 28, 1978
Product Code
GDJ
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GDJ Clamp, Surgical, General & Plastic Surgery

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