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

MADAYAG, MANGHINI, FRANSEEN, GREEN, TROCAR NEEDLES

K Number: K895457 · Decision Nov 1, 1989
Classifications
1
FEI Numbers
207
Registration Numbers
207
Same Product Code
360
Applicant Total
32
Review Days
57

Basic Information

Device Name
MADAYAG, MANGHINI, FRANSEEN, GREEN, TROCAR NEEDLES
K Number
K895457
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Advance Medical Designs, Inc.
Date Received
September 5, 1989
Decision Date
November 1, 1989
Product Code
KNW
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
KNW Instrument, Biopsy

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