K950872 is an FDA 510(k) clearance for the CARDON PHYSICAL THERAPY TABLE MODEL: R27841. This device is classified as a Table, Powered (Class I - General Controls, product code INQ).
Submitted by Cardon Rehabilitation Products, Inc. (Niagara Falls, US). The FDA issued a Cleared decision on May 25, 1995, 86 days after receiving the submission on February 28, 1995.
This device falls under the Physical Medicine FDA review panel. Regulated under 21 CFR 890.3760.
| 510(k) Number | K950872 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 28, 1995 |
| Decision Date | May 25, 1995 |
| Days to Decision | 86 days |
| Submission Type | Traditional |
| Review Panel | Physical Medicine (PM) |
| Summary | Summary PDF |
| Product Code | INQ — Table, Powered |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 890.3760 |