The following data is part of a premarket notification filed by Pie Medical with the FDA for Picus, Parus, Falco And Aquila Ultrasound Systems.
Device ID | K041675 |
510k Number | K041675 |
Device Name: | PICUS, PARUS, FALCO AND AQUILA ULTRASOUND SYSTEMS |
Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
Applicant | PIE MEDICAL 7992 CASTLEWAY DRIVE Indianapolis, IN 46250 |
Contact | Carri Graham |
Correspondent | Carri Graham PIE MEDICAL 7992 CASTLEWAY DRIVE Indianapolis, IN 46250 |
Product Code | IYN |
Subsequent Product Code | ITX |
Subsequent Product Code | IYO |
CFR Regulation Number | 892.1550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-06-21 |
Decision Date | 2004-07-23 |
Summary: | summary |