The following data is part of a premarket notification filed by Vitalcor, Inc. with the FDA for Vitalcor Featherweight Vascular Clamps.
| Device ID | K070661 |
| 510k Number | K070661 |
| Device Name: | VITALCOR FEATHERWEIGHT VASCULAR CLAMPS |
| Classification | Clamp, Vascular |
| Applicant | VITALCOR, INC. PO BOX 7007 Deerfield, IL 60015 |
| Contact | Daniel Kamm |
| Correspondent | Daniel Kamm VITALCOR, INC. PO BOX 7007 Deerfield, IL 60015 |
| Product Code | DXC |
| CFR Regulation Number | 870.4450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-03-09 |
| Decision Date | 2007-08-29 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00851321006550 | K070661 | 000 |
| 00851321006543 | K070661 | 000 |
| 00851321006536 | K070661 | 000 |
| 00851321006529 | K070661 | 000 |
| 00851321006512 | K070661 | 000 |
| 00851321006505 | K070661 | 000 |
| 00851321006499 | K070661 | 000 |