The following data is part of a premarket notification filed by Cancer Technologies, Inc. with the FDA for Extravakit For Radiological Applications.
| Device ID | K883220 |
| 510k Number | K883220 |
| Device Name: | EXTRAVAKIT FOR RADIOLOGICAL APPLICATIONS |
| Classification | Syringe, Piston |
| Applicant | CANCER TECHNOLOGIES, INC. C/O EXTRAVAKIT, INC. 209 S. TUCSON BLVD., BLDG B Tucson, AR 85716 |
| Contact | Dorr, Ph.d |
| Correspondent | Dorr, Ph.d CANCER TECHNOLOGIES, INC. C/O EXTRAVAKIT, INC. 209 S. TUCSON BLVD., BLDG B Tucson, AR 85716 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-07-29 |
| Decision Date | 1988-10-20 |