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

LAPAROSCOPIC KNITTER

K Number: K955490 · Decision Jan 22, 1996
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
23
Review Days
80

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Basic Information

Device Name
LAPAROSCOPIC KNITTER
K Number
K955490
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Core Dynamics, Inc.
Date Received
November 3, 1995
Decision Date
January 22, 1996
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

Similar 510(k) Clearances

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Other Clearances by Core Dynamics, Inc.

K Number Device Name
K992250 CORE AUDIBLE TROCAR II
K992190 CORE POUCH
K953903 LAPAROSCOPIC TROCAR OBTURATOR, 5MM, 10/11MM, 10/12MM
K953409 LAPAROSCOPIC TROCAR
K950457 CANNUAL AND TROCAR, SUPERPUBIC
K943172 CORE DYNAMICS' LAPAROSCOPIC SMOKE ELIMINATOR
K935826 LAPAROSCOPIC/SUCTION/IRRIGATION PROBE
K932118 ENDOSCOPIC TRANSMURAL SUTURE NEEDLE SET
K932021 ENTREE CANNULA FASCIA ANCHORS
K932020 ENTREE BLUNT TIP TROCAR AND ADAPTER
Search all 23 clearances from Core Dynamics, Inc. →