The following data is part of a premarket notification filed by Konigsberg Instruments, Inc. with the FDA for P51 Angioplasty Pressure Transducer.
| Device ID | K813331 |
| 510k Number | K813331 |
| Device Name: | P51 ANGIOPLASTY PRESSURE TRANSDUCER |
| Classification | Catheter, Angioplasty, Peripheral, Transluminal |
| Applicant | KONIGSBERG INSTRUMENTS, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | LIT |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-11-24 |
| Decision Date | 1981-12-29 |