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 13, 2026, FDA's public records list Catalyst Research Corp. with 9 510(k) clearances. The most recent is a 510(k) clearance dated May 28, 1991: MINIOX V PULSE OXIMETER.
| Date | Record | Source |
|---|---|---|
| May 28, 1991 | MINIOX V PULSE OXIMETERK905310 · DQA | 510(k) clearances |
| Jan 19, 1988 | MINIOX IV PORTABLE PULSE OXIMETERK874132 · DQA | 510(k) clearances |
| Aug 28, 1986 | MINIOX 100 PULSE OXIMETERK862798 · DQA | 510(k) clearances |
| Dec 12, 1983 | MINI OX IIK833995 · CCL | 510(k) clearances |
| Nov 3, 1983 | MINI OX III OXYGEN MONITORK833326 · BXL | 510(k) clearances |
| Apr 27, 1979 | MODEL M25RL, (CRC) OXYGEN ANALYZERK790785 · CCL | 510(k) clearances |
| Apr 27, 1979 | MODEL M25R, OXYGEN ANALYZERK790784 · CCL | 510(k) clearances |
| Feb 15, 1979 | ANALYZER, OXYGEN MODEL M25RA & M25RADK782062 · CCL | 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
