# Kai Sensors, Inc.

- Location (FDA's records): Honolulu, HI
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: BZQ (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Welch Allyn Protocol, Inc.: 1 (https://510kreport.com/company/welch-allyn-protocol)
- Medcare Flaga: 1 (https://510kreport.com/company/medcare-flaga)
- Embla Systems: 1 (https://510kreport.com/company/embla-systems)
- Ferguson Medical: 1 (https://510kreport.com/company/ferguson-medical)

## Firms that cite its devices most
- Pneumacare Limited: 1 (https://510kreport.com/company/pneumacare)
- Biancamed Limited: 1 (https://510kreport.com/company/biancamed)
- Kai Medical, Inc.: 1 (https://510kreport.com/company/kai-medical)

## Its most-cited devices
- K090273: Kai Sensors Non-Contact Respiratory Rate Spot Check, Model 100, Kai Rspot, Model 100 (2009), cited by 3

## Recent decisions
- K090273: Kai Sensors Non-Contact Respiratory Rate Spot Check, Model 100, Kai Rspot, Model 100 (Jun 5, 2009)

Source page: https://510kreport.com/company/kai-sensors