The following data is part of a premarket notification filed by Capintec Instruments, Inc. with the FDA for Beta C Counter.
| Device ID | K943072 |
| 510k Number | K943072 |
| Device Name: | BETA C COUNTER |
| Classification | Calibrator, Dose, Radionuclide |
| Applicant | CAPINTEC INSTRUMENTS, INC. 540 ALPHA DR. Pittsburgh, PA 15238 |
| Contact | Mary A Dell, M.s. |
| Correspondent | Mary A Dell, M.s. CAPINTEC INSTRUMENTS, INC. 540 ALPHA DR. Pittsburgh, PA 15238 |
| Product Code | KPT |
| CFR Regulation Number | 892.1360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-06-28 |
| Decision Date | 1994-09-29 |