The following data is part of a premarket notification filed by Vickers America Medical Corp. with the FDA for Vickers Medical Model 112 Treonic Dc2.
| Device ID | K791645 |
| 510k Number | K791645 |
| Device Name: | VICKERS MEDICAL MODEL 112 TREONIC DC2 |
| Classification | Tip, Vessel |
| Applicant | VICKERS AMERICA MEDICAL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FKW |
| CFR Regulation Number | 876.5540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-08-23 |
| Decision Date | 1979-10-02 |