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 Interspec with 17 510(k) clearances. The most recent is a 510(k) clearance dated Nov 22, 1994: INTERSPEC APOGEE RX400 ULTRASOUND IMAGING SYSTEM AND DOPPLER ULTRASOUND FLOWMETER.
| Nov 22, 1994 | INTERSPEC APOGEE RX400 ULTRASOUND IMAGING SYSTEM AND DOPPLER ULTRASOUND FLOWMETERK940671 · ITX | 510(k) clearances |
| Jun 14, 1993 | INTERSPEC APOGEE CLAK924231 · IYO | 510(k) clearances |
| Nov 24, 1992 | INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDEK915696 · ITX | 510(k) clearances |
| Apr 2, 1992 | ULTRASOUND IMAGAING SYSTEM AND DOPPLER FLOWMETERK920678 · ITX | 510(k) clearances |
| Jun 6, 1991 | PROBE REFILL KITK911073 · ITX | 510(k) clearances |
| Apr 29, 1991 | INTERSPEC APOGEE, MODIFICATIONK910049 · DPW | 510(k) clearances |
| Nov 16, 1990 | INTERSPEC APOGEEK903839 · DXK | 510(k) clearances |
| Oct 5, 1990 | INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLERK900155 · ITX | 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
