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

CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS

K Number: K911180 · Decision Mar 29, 1991
Classifications
1
FEI Numbers
653
Registration Numbers
653
Same Product Code
72
Applicant Total
51
Review Days
11

Basic Information

Device Name
CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS
K Number
K911180
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
NORTHGATE TECHNOLOGIES, INC.
Date Received
March 18, 1991
Decision Date
March 29, 1991
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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