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 Criticare Systems, Inc. with 22 510(k) clearances. The most recent is a 510(k) clearance dated Sep 1, 2010: VITAL SIGNS MONITOR.
| Date | Record | Source |
|---|---|---|
| Sep 1, 2010 | VITAL SIGNS MONITORK101602 · MLD | 510(k) clearances |
| May 27, 2009 | 506CN PATIENT MONITORK091050 · DRT | 510(k) clearances |
| Sep 29, 2004 | 8600 VITAL SIGNS MONITORK042569 · MWI | 510(k) clearances |
| Apr 17, 2003 | VITAL SIGNS MONITOR W/ARRHYTHMIA DETECTION AND ST ANALYSIS, MODEL 8100K030613 · MHX | 510(k) clearances |
| Aug 14, 2002 | 507EL VITAL SIGNS MONITORK022435 · DRT | 510(k) clearances |
| Aug 1, 2001 | 8100/8500 VITAL SIGNS MONITORK012059 · MWI | 510(k) clearances |
| Apr 28, 2000 | 8100 VITAL SIGNS MONITORK001020 · MWI | 510(k) clearances |
| Mar 1, 2000 | MPT 24 AND VITAL VIEW 24K000276 · DRG | 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
