# Applied Medical Devices, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 11 (1979–1984): 11 510(k) clearances
- Product codes: FMF (2), FMI (1), IYO (1), GDM (1), KOD (1), KDD (1), KHE (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
- K843885: Percutaneous Aspiration Biopsy Tray (Dec 19, 1984)
- K843883: Sterile Percutaneous Transhepatic Cholan (Dec 13, 1984)
- K843884: General Utility Tray System (Dec 13, 1984)
- K840904: Accu-Cult Fecal Occult Blood Test (Aug 16, 1984)
- K842591: Ultrasound Probe Covers-Sterile (Jul 23, 1984)
- K833720: Transthoracic/Transabdominal-Tray (May 30, 1984)
- K840334: Chemonucleolysis/Discography Tray (Apr 13, 1984)
- K833438: Prepacell-Sterile-Bone Marrow Aspir (Feb 9, 1984)

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