The following data is part of a premarket notification filed by Acuson Corp. with the FDA for Modification Of Acuson V510b Transducer.
| Device ID | K933663 |
| 510k Number | K933663 |
| Device Name: | MODIFICATION OF ACUSON V510B TRANSDUCER |
| Classification | Transducer, Ultrasonic, Diagnostic |
| 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 | ITX |
| CFR Regulation Number | 892.1570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-07-28 |
| Decision Date | 1994-01-21 |