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

LOOSE BODY GRASPERS

K Number: K870881 · Decision Mar 23, 1987
Classifications
1
FEI Numbers
653
Registration Numbers
653
Same Product Code
72
Applicant Total
14
Review Days
18

Basic Information

Device Name
LOOSE BODY GRASPERS
K Number
K870881
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
BOWEN & COMPANY, INC.
Date Received
March 5, 1987
Decision Date
March 23, 1987
Product Code
HTD
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
HTD Forceps

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K863146 BOWEN SUTURE PASSER
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