The following data is part of a premarket notification filed by Carbon Medical Technologies, Inc. with the FDA for Biomarc Tissue Marker.
| Device ID | K032347 |
| 510k Number | K032347 |
| Device Name: | BIOMARC TISSUE MARKER |
| Classification | Staple, Implantable |
| Applicant | CARBON MEDICAL TECHNOLOGIES, INC. 1290 HAMMOND RD. St. Paul, MN 55110 |
| Contact | Robert W Johnson |
| Correspondent | Robert W Johnson CARBON MEDICAL TECHNOLOGIES, INC. 1290 HAMMOND RD. St. Paul, MN 55110 |
| Product Code | GDW |
| CFR Regulation Number | 878.4750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-07-30 |
| Decision Date | 2003-08-21 |
| Summary: | summary |