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

MODIFIED BIOPSY NEEDLE

K Number: K951229 · Decision Apr 6, 1995
Classifications
1
FEI Numbers
198
Registration Numbers
198
Same Product Code
353
Applicant Total
15
Review Days
17

Basic Information

Device Name
MODIFIED BIOPSY NEEDLE
K Number
K951229
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BIOPSYS MEDICAL, INC.
Date Received
March 20, 1995
Decision Date
April 6, 1995
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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K Number Device Name
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K960019 RETRACTOR ARM CLAMP
K953880 BIOPSY NEEDLE
K953962 FORCEPS
K951326 BIOPSY DEVICE ACCESSORY
K950006 SURGICAL STAPLE MARKER
K943863 NEEDLE GUIDE
K945573 BIOPSY DEVICE ACCESSORY
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