K921695 is an FDA 510(k) clearance for the ULTRA COVER ULTRASOUND TRANSDUCER PROBE COVERS. This device is classified as a Transducer, Ultrasonic, Diagnostic (Class II - Special Controls, product code ITX).
Submitted by Parker Laboratories, Inc. (Orange, US). The FDA issued a Cleared decision on February 23, 1995, 1051 days after receiving the submission on April 8, 1992.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1570.
| 510(k) Number | K921695 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 08, 1992 |
| Decision Date | February 23, 1995 |
| Days to Decision | 1051 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Statement |
| Product Code | ITX — Transducer, Ultrasonic, Diagnostic |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1570 |