# Intl. Medical Devices, Ltd.

- Location (FDA's records): Los Angeles, CA
- FDA decisions: 12 (1979–1992): 12 510(k) clearances
- Product codes: BTO (3), GBX (2), FMF (2), FOZ (1), BWC (1), BZQ (1), DRB (1), KGZ (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
- K913540: Pedia-Thor Thoracostomy Kit (Apr 9, 1992)
- K913541: Neo-Thor Thoracostomy Kit (Apr 9, 1992)
- K913542: Thoracic Catheter with Guide (Jan 21, 1992)
- K913539: Thoracic Cathter Stylet (Jan 21, 1992)
- K913543: Thoracic Catheter Stylet (Oct 4, 1991)
- K862909: RE-Trake Weiss Emergency Airway & Thoracic System (Sep 9, 1986)
- K850398: NU-Cath Emergency Kit (Mar 27, 1985)
- K843785: Wisss Pediatric Trach- Tube W/Obturator (Oct 23, 1984)

Source page: https://510kreport.com/company/intl-medical-devices