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

BIFURCATED SUCTION/IRRIGAT TUBING SET W/PUSH BUTTO

K Number: K926477 · Decision Nov 12, 1993
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
16
Applicant Total
23
Review Days
318

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Basic Information

Device Name
BIFURCATED SUCTION/IRRIGAT TUBING SET W/PUSH BUTTO
K Number
K926477
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Core Dynamics, Inc.
Date Received
December 29, 1992
Decision Date
November 12, 1993
Product Code
GBW
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
GBW Catheter, Peritoneal

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
K955490 LAPAROSCOPIC KNITTER
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
Search all 23 clearances from Core Dynamics, Inc. →