# K & S Medicorp

- Location (FDA's records): Miami, FL
- FDA decisions: 3 (1986–1986): 3 510(k) clearances
- Product codes: LDE (1), DQD (1), BZT (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
- K862131: Saltzman Ear (TM) Endotracheal Ascultation Receptor (Jul 14, 1986)
- K854772: Transcor (TM) Radio-Stethoscope (May 13, 1986)
- K854771: Saltzman Stethoscope Head (May 9, 1986)

Source page: https://510kreport.com/company/k-s-medicorp