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

SELECTA-TIP LAPAROSCOPIC SCISSORS

K Number: K970826 · Decision Mar 28, 1997
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
12
Review Days
22

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Basic Information

Device Name
SELECTA-TIP LAPAROSCOPIC SCISSORS
K Number
K970826
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Microline Pentax, Inc.
Date Received
March 6, 1997
Decision Date
March 28, 1997
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

Similar 510(k) Clearances

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Other Clearances by Microline Pentax, Inc.

K Number Device Name
K013695 MICROLINE INC. REUSABLE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM CLIPS, MODEL M/L-10
K982984 ACCUSHEAR LAPAROSCOPIC SURGICAL INSTRUMENTS
K981389 DISPOSABLE RE-NEW FORCEPS
K981188 ELECTROSURGICAL CAUTERY PROBES
K980758 3 MM SELEC-TIP LAPAROSCOPIC SCISSORS
K974066 RE-NEW FORCEPS LAPAROSCOPIC SURGICAL TIPS
K962119 RE-NEW LAPAROSCOPIC INSTRUMENTS
K932648 QUICK SWITCH LAPAROSCOPIC INSTRUMENTS
K897093 INTRAOCULAR MICROSCISSORS BY MEANS OF GAMMA RADIA.
K881049 BRADBURY INTRAOCULAR RETINAL KIT CAT #200
Search all 12 clearances from Microline Pentax, Inc. →