Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list General Theraphysical with 7 510(k) clearances. The most recent is a 510(k) clearance dated Oct 3, 1978: DYNATRON 406 ELECTROTHERAPY APPARATUS.
| Oct 3, 1978 | DYNATRON 406 ELECTROTHERAPY APPARATUSK781318 · IPF | 510(k) clearances |
| Oct 3, 1978 | THERAPY APPAR. 422 INTERFERENTIALK781319 · IPF | 510(k) clearances |
| Oct 3, 1978 | MUSCLE STIMULATION APPARATUSK781315 · IPF | 510(k) clearances |
| Oct 3, 1978 | ULTRASONIC THERAPY APPARATUS, 407K781317 · IMI | 510(k) clearances |
| Oct 3, 1978 | THERAPY UNIT & ELECTRODIAG.K781314 · GXY | 510(k) clearances |
| Sep 27, 1978 | SHORTWAVE THERAPY APPAR. CURAMED 401K781320 · IMJ | 510(k) clearances |
| Sep 27, 1978 | PULSED AND CONTINUOUS SHORTWAVE APPAR.K781316 · IMJ | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
