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 Intertech/Ohio with 10 510(k) clearances. The most recent is a 510(k) clearance dated Oct 19, 1989: INTERTECH METERED DOSE ELBOW.
| Oct 19, 1989 | INTERTECH METERED DOSE ELBOWK895144 · BZA | 510(k) clearances |
| Mar 1, 1989 | INTERTECH UNIVERSAL HYDROPHOBIC FILTERK890346 · CAH | 510(k) clearances |
| Dec 16, 1988 | PEDIATRIC HUMIDIFIER TUBE W/ TEMPERATURE PORTK884525 · BZO | 510(k) clearances |
| Nov 16, 1988 | ADULT RESUSCITATOR WITH MASK AND FILTERK884526 · BTM | 510(k) clearances |
| Jul 8, 1988 | RESUSCITATOR VALVE ASSEMBLY W/FILTERK882204 · CBP | 510(k) clearances |
| Feb 29, 1988 | FIRST RESPONSE PEDIATRIC EMERGENCY RESUSCITATORK880394 · BTM | 510(k) clearances |
| Aug 20, 1986 | PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONSK863033 · BZO | 510(k) clearances |
| Jun 30, 1986 | HEAT/MOISTURE EXCHANGER, HME, W/INTEGRAL FILTERK862020 · BYD | 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
