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 Heyer-Schulte Corp. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Nov 16, 1979: 2 FR KELMAN CHAMBER MAINTAINER.
| Nov 16, 1979 | 2 FR KELMAN CHAMBER MAINTAINERK792096 · FMI | 510(k) clearances |
| Aug 3, 1979 | SUBCUTANEOUS TISSUE EXPANDERK790842 · LCJ | 510(k) clearances |
| Sep 7, 1978 | LUMBAR NERVE ROOT SHIELDK780706 · | 510(k) clearances |
| Apr 18, 1978 | ASEPTIC TRANSFER SETK780417 · GAZ | 510(k) clearances |
| Oct 11, 1977 | RADOVAN SUBCUTANEOUS TISSUE EXPANDERK771224 · LCJ | 510(k) clearances |
| Nov 3, 1976 | T-TUBE DRAIN, ROUNDK760778 · GCY | 510(k) clearances |
| Nov 1, 1976 | MISHLER 2 CHAMB FLUSHING VALVE,STANDK760784 · JXG | 510(k) clearances |
| Nov 1, 1976 | MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPHK760785 · JXG | 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
