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

ENDOPATH DISPOSABLE PNEUMOPERITONEUM NEEDLE

K Number: K910875 · Decision Mar 19, 1991
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
0
Applicant Total
204
Review Days
18

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Basic Information

Device Name
ENDOPATH DISPOSABLE PNEUMOPERITONEUM NEEDLE
K Number
K910875
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
ETHICON, Inc.
Date Received
March 1, 1991
Decision Date
March 19, 1991
Product Code
FDP
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
FDP Apparatus, Pneumoperitoneum, Automatic

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