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 |