The following data is part of a premarket notification filed by Philips Ultrasound, Inc. with the FDA for 5 Mhz Doppler Outrigger.
Device ID | K872817 |
510k Number | K872817 |
Device Name: | 5 MHZ DOPPLER OUTRIGGER |
Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
Applicant | PHILIPS ULTRASOUND, INC. 2722 S. FAIRVIEW Santa Ana, CA 92704 |
Contact | Martin A Kaufman |
Correspondent | Martin A Kaufman PHILIPS ULTRASOUND, INC. 2722 S. FAIRVIEW Santa Ana, CA 92704 |
Product Code | IYN |
CFR Regulation Number | 892.1550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-07-16 |
Decision Date | 1988-02-08 |