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 HalmaLabelled 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 15, 2026, FDA's public records list Sensidyne with 4 510(k) clearances. The most recent is a 510(k) clearance dated May 13, 2002: SENSAID, MODELS# RC-NVA30-10; RC-CS140-10; RC-BC150-3.
| May 13, 2002 | SENSAID, MODELS# RC-NVA30-10; RC-CS140-10; RC-BC150-3K021246 · DQA | 510(k) clearances |
| Feb 12, 2002 | SENSAIDK011974 · DQA | 510(k) clearances |
| Mar 1, 2001 | 100 SERIES OXYGEN ANALYZER, MODELS 1000-E AND 1000-IK010382 · CCL | 510(k) clearances |
| Aug 31, 2000 | SENSIDYNE OXYGEN ANALYZER & SENSIDYNE OXYGEN MONITORK000700 · 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
