The following data is part of a premarket notification filed by Millar Instruments, Inc. with the FDA for Millar Mikro-tip Catheter Pressure Tran..
| Device ID | K812944 |
| 510k Number | K812944 |
| Device Name: | MILLAR MIKRO-TIP CATHETER PRESSURE TRAN. |
| Classification | Catheter, Electrode Recording, Or Probe, Electrode Recording |
| Applicant | MILLAR INSTRUMENTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DRF |
| CFR Regulation Number | 870.1220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-10-20 |
| Decision Date | 1981-11-16 |