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

BIOPSY INTRODUCER NEEDLE

K Number: K963390 · Decision Oct 10, 1996
Classifications
1
FEI Numbers
198
Registration Numbers
198
Same Product Code
353
Applicant Total
503
Review Days
43

Basic Information

Device Name
BIOPSY INTRODUCER NEEDLE
K Number
K963390
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BAXTER HEALTHCARE CORP.
Date Received
August 28, 1996
Decision Date
October 10, 1996
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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