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

ENTREE BLUNT TIP TROCAR AND ADAPTER

K Number: K932020 · Decision Jan 11, 1994
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
23
Review Days
263

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Basic Information

Device Name
ENTREE BLUNT TIP TROCAR AND ADAPTER
K Number
K932020
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Core Dynamics, Inc.
Date Received
April 23, 1993
Decision Date
January 11, 1994
Product Code
HET
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HET Laparoscope, Gynecologic (And Accessories)

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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
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