Submission Details
| 510(k) Number | K882917 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 12, 1988 |
| Decision Date | July 28, 1988 |
| Days to Decision | 16 days |
| Submission Type | Traditional |
| Review Panel | Physical Medicine (PM) |
| Summary | — |
K882917 is an FDA 510(k) clearance for the HI-LO TABLE, MODEL 820-05, a Table, Physical Therapy, Multi Function (Class II — Special Controls, product code JFB), submitted by Tri W-G, Inc. (Valley City, US). The FDA issued a Cleared decision on July 28, 1988, 16 days after receiving the submission on July 12, 1988. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.5880.
| 510(k) Number | K882917 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 12, 1988 |
| Decision Date | July 28, 1988 |
| Days to Decision | 16 days |
| Submission Type | Traditional |
| Review Panel | Physical Medicine (PM) |
| Summary | — |
| Product Code | JFB — Table, Physical Therapy, Multi Function |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 890.5880 |