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., part of Johnson & JohnsonLabelled 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. See the Johnson & Johnson group view.
As of Nov 13, 2026, FDA's public records list Critikon with 51 510(k) clearances. The most recent is a 510(k) clearance dated Sep 21, 2000: DINAMAP PRO 1000 MONITOR, MODEL 1000.
| Date | Record | Source |
|---|---|---|
| Sep 21, 2000 | DINAMAP PRO 1000 MONITOR, MODEL 1000K002248 · DXN | 510(k) clearances |
| May 26, 2000 | DINAMAP ADVANCED NIBP MODULEK000500 · DXN | 510(k) clearances |
| Feb 24, 2000 | DINAMAP PRO SERIES MONITOR, MODELS 100, 200, 300, 400K992638 · MWI | 510(k) clearances |
| Aug 14, 1998 | DINAMAP MPS SELECT PORTABLE MONITORK982342 · MSX | 510(k) clearances |
| Jun 16, 1995 | DINAMAP PLUS VITAL SIGNS MONOITORK943709 · DPS | 510(k) clearances |
| Mar 1, 1995 | DINAMAP VITAL SIGNS MONITOR MODELS 9300 AND 9320/9340K942700 · MHX | 510(k) clearances |
| Feb 9, 1994 | CRITIKON CENTRAL STATIN MONITORK933404 · DPS | 510(k) clearances |
| Dec 14, 1993 | CHANGES TO PROTECTIV(TM) & JELCO(TM) WINGED CATHK933050 · FOZ | 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
