The following data is part of a premarket notification filed by Cancer Technologies, Inc. with the FDA for Extravakit.
| Device ID | K874807 |
| 510k Number | K874807 |
| Device Name: | EXTRAVAKIT |
| Classification | Syringe, Piston |
| Applicant | CANCER TECHNOLOGIES, INC. P.O. BOX 12865 TUCSON, AZ 85732 |
| Contact | DORR, PHD |
| Correspondent | DORR, PHD CANCER TECHNOLOGIES, INC. P.O. BOX 12865 TUCSON, AZ 85732 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent - With Drug (SESD) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-11-20 |
| Decision Date | 1988-02-04 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() EXTRAVAKIT 73751873 1540327 Dead/Cancelled |
EXTRAVAKIT, INC. 1988-09-14 |