# Mon-A-Therm, Inc.

- Location (FDA's records): St. Louis, MO
- FDA decisions: 17 (1982–1989): 17 510(k) clearances
- Product codes: FLL (11), GEI (1), CAI (1), KRB (1), KPD (1), BZW (1), KOD (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K885187: Model 1000 Electronic Clinical Thermometer (Mar 8, 1989)
- K874522: Modified Myocardial Temperature Sensor (Jan 29, 1988)
- K874519: Modified Esophageal Stethoscope/Temperature Sensor (Jan 29, 1988)
- K875234: Mon-a-Therm's Skin Temperature Sensor (Jan 19, 1988)
- K874524: Modified Subcutaneous Temperature Sensor (Jan 6, 1988)
- K874523: Modified Tympanic & Esophageal/Rectal Temp. Sensor (Jan 6, 1988)
- K874520: Modified Airway Temperature Sensor (Jan 6, 1988)
- K874521: Modified Thermal Well Temperature Sensor (Jan 6, 1988)

Source page: https://510kreport.com/company/mon-a-therm