Diagnostics 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 In-Line Diagnostics Corp. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Dec 20, 2000: CRIT-LINE MONITOR III (CLM III).
| Dec 20, 2000 | CRIT-LINE MONITOR III (CLM III)K001763 · MQS | 510(k) clearances |
| Jul 30, 1999 | CRIT-LINE MONITOR III (CLM III)K992227 · MQS | 510(k) clearances |
| May 27, 1999 | CRIT-SCAN II MONITORK983551 · GKF | 510(k) clearances |
| Oct 9, 1998 | MODIFICATION OF CRIT-LINE MONITOR III (CLM III)K982412 · MQS | 510(k) clearances |
| Dec 11, 1997 | CRIT-LINE MONITOR (CLMIII)K972470 · MQS | 510(k) clearances |
| Jul 23, 1996 | CRIT-LINE HEMATOCRIT ALERT (MODIFICATION)K953875 · MQS | 510(k) clearances |
| Mar 14, 1995 | CRIT-LINE HEMATOCRIT ALERTK950942 · JPI | 510(k) clearances |
| Jan 19, 1995 | CRIT-LINE BLOOD CHAMBER WITH E-BEAMK935958 · KOC | 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
