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

SKIN STAPLE REMOVER

K Number: K810785 · Decision Apr 10, 1981
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
66
Applicant Total
1
Review Days
18

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Basic Information

Device Name
SKIN STAPLE REMOVER
K Number
K810785
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Rowley Mfg. Co.
Date Received
March 23, 1981
Decision Date
April 10, 1981
Product Code
KDC
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
KDC Instrument, Surgical, Disposable

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