# Shotwell & Carr, Inc.

- Location (FDA's records): Dallas, TX
- FDA decisions: 3 (1995–1997): 3 510(k) clearances
- Product codes: KGI (1), JOY (1), IPF (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
- K970824: MDX 2000, Digital Analyzer (May 30, 1997)
- K961011: DTX-200 Bone Densitometer (Jul 5, 1996)
- K950617: Smart Wave GS100 (Oct 13, 1995)

Source page: https://510kreport.com/company/shotwell-carr