# Kma, Inc.

- Location (FDA's records): Bethesda, MD
- FDA decisions: 3 (1980–1985): 3 510(k) clearances
- Product codes: FLL (1), DYG (1), KRB (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
- K850395: The Fever-Therm a Therm. Measuring Device (Aug 13, 1985)
- K821099: Heparin Coated Thermodilution Catheter (May 18, 1982)
- K800836: Kma Flow Directed Thermodilution Cathete (Apr 24, 1980)

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