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

ENTREE CANNULA FASCIA ANCHORS

K Number: K932021 · Decision Jan 11, 1994
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
8
Applicant Total
23
Review Days
263

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Basic Information

Device Name
ENTREE CANNULA FASCIA ANCHORS
K Number
K932021
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.5090
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Core Dynamics, Inc.
Date Received
April 23, 1993
Decision Date
January 11, 1994
Product Code
FBM
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FBM Cannula And Trocar, Suprapubic, Non-Disposable

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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
K932020 ENTREE BLUNT TIP TROCAR AND ADAPTER
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