K780229 is an FDA 510(k) clearance for the ABDOMINAL BELT. This device is classified as a Orthosis, Abdominal (Class I - General Controls, product code KTD).
Submitted by Biomet, Inc. (Mchenry, US). The FDA issued a Cleared decision on March 2, 1978, 21 days after receiving the submission on February 9, 1978.
This device falls under the Physical Medicine FDA review panel. Regulated under 21 CFR 890.3490.
| 510(k) Number | K780229 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 09, 1978 |
| Decision Date | March 02, 1978 |
| Days to Decision | 21 days |
| Submission Type | Traditional |
| Review Panel | Physical Medicine (PM) |
| Summary | — |
| Product Code | KTD — Orthosis, Abdominal |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 890.3490 |