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

MICROMARK II TISSUE MARKER,MODEL C1535

K Number: K013413 · Decision Dec 3, 2001
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
104
Applicant Total
111
Review Days
49

Basic Information

Device Name
MICROMARK II TISSUE MARKER,MODEL C1535
K Number
K013413
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ETHICON ENDO-SURGERY, INC.
Date Received
October 15, 2001
Decision Date
December 3, 2001
Product Code
NEU
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
NEU Marker, Radiographic, Implantable

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