FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

TISSUE GRASPING FORCEPS, SCISSORS, CLAMPS AND DISSECTORS FOR LAPAROSCOPIC SURGERIES

K Number: K012725 · Decision Nov 8, 2001
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
7
Review Days
85

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Basic Information

Device Name
TISSUE GRASPING FORCEPS, SCISSORS, CLAMPS AND DISSECTORS FOR LAPAROSCOPIC SURGERIES
K Number
K012725
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Endo-Therapeutics, Inc.
Date Received
August 15, 2001
Decision Date
November 8, 2001
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

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K090796 MULTI-BITE HOT BIOPSY FORCEPS
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K023603 ENDO-GLIDE GUIDEWIRE
K012977 VARICES INJECTION NEEDLE
K926549 ENDOCATH ELECTROPHYSIOLOGY CATHETER
K925392 BIOPSY FORCEPS