FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

FORCEPS

K Number: K953962 · Decision Sep 8, 1995
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
15
Review Days
17

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Basic Information

Device Name
FORCEPS
K Number
K953962
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biopsys Medical, Inc.
Date Received
August 22, 1995
Decision Date
September 8, 1995
Product Code
GEN
Advisory Committee
General, Plastic Surgery
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
GEN Forceps, General & Plastic Surgery

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Other Clearances by Biopsys Medical, Inc.

K Number Device Name
K970817 MICROMARK CLIP
K970565 MAMMOTOME BIOPSY PROBE AND HOUSING (MAMMOTOME)
K963015 SURGICAL STAPLE MARKER DEVICE (MODIFY)
K960019 RETRACTOR ARM CLAMP
K953880 BIOPSY NEEDLE
K951326 BIOPSY DEVICE ACCESSORY
K951229 MODIFIED BIOPSY NEEDLE
K950006 SURGICAL STAPLE MARKER
K943863 NEEDLE GUIDE
K945573 BIOPSY DEVICE ACCESSORY
Search all 15 clearances from Biopsys Medical, Inc. →