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

LOWMAN BONE FORCEP

K Number: K771192 · Decision Jul 11, 1977
Classifications
1
FEI Numbers
658
Registration Numbers
658
Same Product Code
72
Applicant Total
140
Review Days
10

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Basic Information

Device Name
LOWMAN BONE FORCEP
K Number
K771192
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
July 1, 1977
Decision Date
July 11, 1977
Product Code
HTD
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
HTD Forceps

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