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 13, 2026, FDA's public records list Monitor Science Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated May 25, 1979: RIA KIT, PROSTATIC ACID.
| Date | Record | Source |
|---|---|---|
| May 25, 1979 | RIA KIT, PROSTATIC ACIDK790580 · JFH | 510(k) clearances |
| Aug 14, 1978 | BIO-MONITOR AMIKACINK780949 · KLP | 510(k) clearances |
| Aug 14, 1978 | BIO-MONITOR TOBRAMYCINK780950 · DID | 510(k) clearances |
| Aug 14, 1978 | BIO-MONITOR GENTAMICINK780951 · DKD | 510(k) clearances |
| Jan 12, 1978 | KANAMYCIN RIAK772038 · KJI | 510(k) clearances |
| Nov 23, 1977 | BETA-HCG RIAK772039 · JHI | 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
