The following data is part of a premarket notification filed by Acuson Corp. with the FDA for Acuson Model #29001 (diagnostic Ultrasound Device).
| Device ID | K930964 |
| 510k Number | K930964 |
| Device Name: | ACUSON MODEL #29001 (DIAGNOSTIC ULTRASOUND DEVICE) |
| Classification | System, Imaging, Pulsed Echo, Ultrasonic |
| Applicant | ACUSON CORP. 1220 CHARLESTON RD. Mountain View, CA 94039 -7393 |
| Contact | Sheila Pickering |
| Correspondent | Sheila Pickering ACUSON CORP. 1220 CHARLESTON RD. Mountain View, CA 94039 -7393 |
| Product Code | IYO |
| CFR Regulation Number | 892.1560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-02-24 |
| Decision Date | 1994-10-26 |