The following data is part of a premarket notification filed by Pie Medical Equipment B.v. with the FDA for Diagnostic Ultrasound System Model Sc480.
Device ID | K911584 |
510k Number | K911584 |
Device Name: | DIAGNOSTIC ULTRASOUND SYSTEM MODEL SC480 |
Classification | System, Imaging, Pulsed Echo, Ultrasonic |
Applicant | PIE MEDICAL EQUIPMENT B.V. PHILIPSWEG 1 Maastricht, NL 6227 Aj |
Contact | Rikers |
Correspondent | Rikers PIE MEDICAL EQUIPMENT B.V. PHILIPSWEG 1 Maastricht, NL 6227 Aj |
Product Code | IYO |
CFR Regulation Number | 892.1560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-04-08 |
Decision Date | 1991-10-24 |