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

TEW BYPASS INSTRUMENTS & DISSECTING KIT

K Number: K791703 · Decision Oct 4, 1979
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
6
Applicant Total
140
Review Days
37

Basic Information

Device Name
TEW BYPASS INSTRUMENTS & DISSECTING KIT
K Number
K791703
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
August 28, 1979
Decision Date
October 4, 1979
Product Code
GDI
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
GDI Dissector, Surgical, General & Plastic Surgery

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