K935595 is an FDA 510(k) clearance for the ACUSON MODEL 3001. This device is classified as a Transducer, Ultrasonic, Diagnostic (Class II - Special Controls, product code ITX).
Submitted by Acuson Corp. (Mountain View, US). The FDA issued a Cleared decision on March 2, 1995, 468 days after receiving the submission on November 19, 1993.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1570.
| 510(k) Number | K935595 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 19, 1993 |
| Decision Date | March 02, 1995 |
| Days to Decision | 468 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | ITX — Transducer, Ultrasonic, Diagnostic |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1570 |