K894806 is an FDA 510(k) clearance for the SIEMENS ENDO-P-PROBE. This device is classified as a System, Imaging, Pulsed Echo, Ultrasonic (Class II - Special Controls, product code IYO).
Submitted by Siemens Medical Solutions USA, Inc. (Pleasanton, US). The FDA issued a Cleared decision on October 5, 1989, 69 days after receiving the submission on July 28, 1989.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1560.
| 510(k) Number | K894806 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 28, 1989 |
| Decision Date | October 05, 1989 |
| Days to Decision | 69 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | — |
| Product Code | IYO — System, Imaging, Pulsed Echo, Ultrasonic |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1560 |