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

GRASPING FORCEP (W/FOUR PRONGS)

K Number: K792100 · Decision Nov 13, 1979
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
10
Review Days
25

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Basic Information

Device Name
GRASPING FORCEP (W/FOUR PRONGS)
K Number
K792100
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Eder Instrument Co, Inc.
Date Received
October 19, 1979
Decision Date
November 13, 1979
Product Code
GEN
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
GEN Forceps, General & Plastic Surgery

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Other Clearances by Eder Instrument Co, Inc.

K Number Device Name
K843498 BIPOLAR SUCTION ELECTRODE
K843497 SURGICAL KNIVES & PROBES
K843499 ARTHROSCOPY LEG HOLDER
K831255 LARYNGOSCOPE ATTACHMENT PH2000
K831240 LASER BRONCHOSCOPE
K831241 LASER LAPARAXOPE
K822959 ENDOSCOPIC VIDEOSYSTEM
K802479 SURGICAL KNIVES & PROBES
K791052 ENDOSCOPIC INSTRUMENT