Submission Details
| 510(k) Number | K800208 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 01, 1980 |
| Decision Date | February 21, 1980 |
| Days to Decision | 20 days |
| Submission Type | Traditional |
| Review Panel | Physical Medicine (PM) |
| Summary | — |
K800208 is an FDA 510(k) clearance for the SKIL-CARE LEG PADS. This device is classified as a Accessories, Wheelchair (Class I — General Controls, product code KNO).
Submitted by Skil-Care Corp. (Mchenry, US). The FDA issued a Cleared decision on February 21, 1980, 20 days after receiving the submission on February 1, 1980.
This device falls under the Physical Medicine FDA review panel. Regulated under 21 CFR 890.3910.
| 510(k) Number | K800208 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 01, 1980 |
| Decision Date | February 21, 1980 |
| Days to Decision | 20 days |
| Submission Type | Traditional |
| Review Panel | Physical Medicine (PM) |
| Summary | — |
| Product Code | KNO — Accessories, Wheelchair |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 890.3910 |