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 13, 2026, FDA's public records list I-Rep with 8 510(k) clearances. The most recent is a 510(k) clearance dated Feb 2, 1994: LATHAM TABLE.
| Date | Record | Source |
|---|---|---|
| Feb 2, 1994 | LATHAM TABLEK930692 · INQ | 510(k) clearances |
| Jul 22, 1993 | ACCUTRAC TRACTION UNITK930691 · ITH | 510(k) clearances |
| Jul 14, 1986 | MEDTRON TYPE P-300 ULTRASONIC THERAPY UNITK861864 · IMJ | 510(k) clearances |
| Jan 3, 1986 | REHABILITATION TABLESK854947 · INQ | 510(k) clearances |
| May 7, 1985 | ADJUSTABLE TREATMENT TABLESK851690 · | 510(k) clearances |
| Jul 20, 1984 | VACUPULSE VACUUM UNITK842268 · IPF | 510(k) clearances |
| Nov 7, 1983 | ROTAGYMK832940 · ISD | 510(k) clearances |
| Oct 15, 1982 | PHYSICAL MEDICINE & REHABILITATION EQUIPK822906 · ION | 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
