Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 American Diagnostic Corporation with 39 510(k) clearances. The most recent is a 510(k) clearance dated Mar 10, 2017: Adscope 658 Electronic Stethoscope.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Mar 10, 2017 | Adscope 658 Electronic StethoscopeK162589 · DQD | 510(k) clearances |
| Nov 19, 2010 | OTOSCOPE AND OPHTHALMOSCOPE DIAGNOSTIC INSTRUMENT KITSK093495 · HLJ | 510(k) clearances |
| May 15, 2006 | ADSCOPE 657BK ELECTRONIC STETHOSCOPE, MODEL 657BKK060321 · DQD | 510(k) clearances |
| Nov 1, 2001 | ADC 656 ELECTRONIC STETHOSCOPEK012304 · DQD | 510(k) clearances |
| Jan 27, 1997 | ANEROID AND MERCURIAL SPHYGMOMANOMETERSK962655 · DXQ | 510(k) clearances |
| Jul 8, 1994 | ELECTRONIC THERMOMETERSK940686 · FLL | 510(k) clearances |
| Mar 3, 1994 | PROSCOPES AND ADSCOPESK935944 · LDE | 510(k) clearances |
| Oct 18, 1993 | COAGULATION REFERENCE PLASMA, NORMALK932145 · GIZ | 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
