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

GS-1400 TOOTHED DISSECTING FORCEP, 5MM, INSULATED

K Number: K900959 · Decision Apr 18, 1990
Classifications
1
FEI Numbers
70
Registration Numbers
71
Same Product Code
4
Applicant Total
21
Review Days
50

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Basic Information

Device Name
GS-1400 TOOTHED DISSECTING FORCEP, 5MM, INSULATED
K Number
K900959
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Solos Endoscopy, Inc.
Date Received
February 27, 1990
Decision Date
April 18, 1990
Product Code
GEJ
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
GEJ Carrier, Ligature

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Other Clearances by Solos Endoscopy, Inc.

K Number Device Name
K983538 MINIATURIZED BIOPSY,SCOPE A.K.A: BIOPSY NEEDLE WITH ENDOSCOPIC VIEWING CAPABILITY
K910671 MODEL GS-4700 COMMON DUCT STONE REMOVING KIT
K900964 CANNULA AND TROCAR, 11MM
K900957 GS-2100 HOOK SUTURE SCISSOR, 5MM
K900965 GS-4550 TROCAR ONLY, 11MM
K900954 GS-5200 HOOK SUCTION/COAGULATOR, 5MM
K900961 GS-4100 REDUCER SLEEVE, 5MM TO 3MM
K900948 GS-1002 GRASPING FORCEP, 5MM WITH RATCHET
K900953 GS-5000 SPATULA SUCTION/COAGULATOR, 5MM
K900952 GS-1200 GRASPING/EXTRACTING FORCEP, 10MM
Search all 21 clearances from Solos Endoscopy, Inc. →