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 | Device Class | Medical Specialty |
|---|---|---|---|
| NEU | Marker, Radiographic, Implantable | FDA class 2 | General, Plastic Surgery |
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