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

CANNUAL AND TROCAR, SUPERPUBIC

K Number: K950457 · Decision May 5, 1995
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
23
Review Days
91

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CANNUAL AND TROCAR, SUPERPUBIC
K Number
K950457
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
February 3, 1995
Decision Date
May 5, 1995
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)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HET), ordered by most recent decision date.

View all

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
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. →