The following data is part of a premarket notification filed by Bruel & Kjaer Industri A/s with the FDA for Diagnostic Ultrasound System Type 3535, Modified.
| Device ID | K914945 |
| 510k Number | K914945 |
| Device Name: | DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535, MODIFIED |
| Classification | System, Imaging, Pulsed Echo, Ultrasonic |
| Applicant | BRUEL & KJAER INDUSTRI A/S 18 NAERUM HOVEDGADE DK-2850 NAERUM Denmark, DK |
| Contact | Aage Ruby |
| Correspondent | Aage Ruby BRUEL & KJAER INDUSTRI A/S 18 NAERUM HOVEDGADE DK-2850 NAERUM Denmark, DK |
| Product Code | IYO |
| CFR Regulation Number | 892.1560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-11-04 |
| Decision Date | 1992-06-26 |