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

UNITIPS SURGICAL INSTRUMENTS

K Number: K925882 · Decision Aug 10, 1993
Classifications
1
FEI Numbers
573
Registration Numbers
573
Same Product Code
1391
Applicant Total
12
Review Days
264

Basic Information

Device Name
UNITIPS SURGICAL INSTRUMENTS
K Number
K925882
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
UNISURGE, INC.
Date Received
November 19, 1992
Decision Date
August 10, 1993
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
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
GCJ Laparoscope, General & Plastic Surgery

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Other Clearances by UNISURGE, INC.

K Number Device Name
K943502 UNIGRIP
K933720 INSTRUMENT ACTUATING DEVICE (IAD)
K930605 APPLIER, SURGICAL, CLIP
K930617 OBGRIP AND UNITIPS(TM)
K925917 UNICHANNEL(TM SURGICAL GRASPER
K930809 UNITIPS
K932604 UNIGRIP-FH SURGICAL HANDPIECE/LAPAROSCOPIC
K926341 UNITROCAR(TM) REUSABLE SURG TROCAR/RESUSE KIT
K926199 UNICLIP SURGICAL CLIP APPLIER
K914923 UNISURGE DISPOSABLE TROCAR
Search all 12 clearances from UNISURGE, INC. →