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 15, 2026, FDA's public records list Bio Clinic Co. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Aug 6, 1993: AMERICAN POWER CONVERSIONS, BACK-UPS 600.
| Aug 6, 1993 | AMERICAN POWER CONVERSIONS, BACK-UPS 600K930791 · FMF | 510(k) clearances |
| Jul 21, 1993 | PRISMK932480 · IOQ | 510(k) clearances |
| Jun 24, 1993 | ORTHODERM CONSUMMATE AIR THERAPY BED W/SCALEK926189 · IOQ | 510(k) clearances |
| Jul 2, 1992 | ELISA TUBE TSH TESTK921958 · JLW | 510(k) clearances |
| May 27, 1992 | ORTHODERM CONVERTIBLE IIK922140 · IOQ | 510(k) clearances |
| May 7, 1992 | MIRCO ELISA HPL TEST KITK921212 · JHI | 510(k) clearances |
| May 7, 1992 | NOW PREGNANCY TEST KITK921211 · JHI | 510(k) clearances |
| Apr 8, 1992 | ELISA TUBE PROLACTIN TEST KITK920921 · CFT | 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
