# Sensidyne, Inc.

- Location (FDA's records): Clearwater, FL
- FDA decisions: 4 (2000–2002): 4 510(k) clearances
- Product codes: DQA (2), CCL (2)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K011974: Sensaid (2002), cited by 1

## Recent decisions
- K021246: Sensaid, Models# RC-NVA30-10; RC-CS140-10; RC-BC150-3 (May 13, 2002)
- K011974: Sensaid (Feb 12, 2002)
- K010382: 100 Series Oxygen Analyzer, Models 1000-E and 1000-I (Mar 1, 2001)
- K000700: Sensidyne Oxygen Analyzer & Sensidyne Oxygen Monitor (Aug 31, 2000)

Source page: https://510kreport.com/company/sensidyne