FDA 510(k) Applications for Medical Device Product Code "MAA"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K102138 | EDAN INSTRUMENTS, INC. | ULTRASONIC TABLETOP DOPPLER; ULTRASONIC TABLETOP DOPPLER | 10/28/2010 |
K090499 | SUMMIT DOPPLER SYSTEMS, INC. | LIFEDOP MODEL, L350R | 03/31/2009 |