The following data is part of a premarket notification filed by Millar Instruments, Inc. with the FDA for Millar Pulsed Doppler Velocimeter.
| Device ID | K860766 |
| 510k Number | K860766 |
| Device Name: | MILLAR PULSED DOPPLER VELOCIMETER |
| Classification | Flowmeter, Blood, Cardiovascular |
| Applicant | MILLAR INSTRUMENTS, INC. P.O. BOX 18227 Houston, TX 77223 |
| Contact | Robert D Miers |
| Correspondent | Robert D Miers MILLAR INSTRUMENTS, INC. P.O. BOX 18227 Houston, TX 77223 |
| Product Code | DPW |
| CFR Regulation Number | 870.2100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-03-03 |
| Decision Date | 1986-07-29 |