K822992 is an FDA 510(k) clearance for the PEOPLE MOVER. This device is classified as a Chair, With Casters (Class I - General Controls, product code INM).
Submitted by Convaid Products, Inc. (Mchenry, US). The FDA issued a Cleared decision on October 27, 1982, 15 days after receiving the submission on October 12, 1982.
This device falls under the Physical Medicine FDA review panel. Regulated under 21 CFR 890.3100.
| 510(k) Number | K822992 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 12, 1982 |
| Decision Date | October 27, 1982 |
| Days to Decision | 15 days |
| Submission Type | Traditional |
| Review Panel | Physical Medicine (PM) |
| Summary | — |
| Product Code | INM — Chair, With Casters |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 890.3100 |