# The Medi-Dose Group

- Location (FDA's records): Feasterville, PA
- FDA decisions: 10 (1989–1995): 10 510(k) clearances
- Product codes: FPA (6), FMF (3), FPB (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
- K952242: Transfeer Spike II (Sep 15, 1995)
- K942625: 1.2 Micron Air Eliminating Filter (Oct 7, 1994)
- K900651: TS-1800 Medication Transfer Spike (May 7, 1990)
- K895291: IV Dispesnsing Spike (Dec 27, 1989)
- K895290: Chemo-Spike Reconstitution Device (Dec 27, 1989)
- K896291: Injection Port II --- for Intermittent Injection (Dec 1, 1989)
- K895419: Disposable Disc Filter (Nov 24, 1989)
- K892429: Injection Port for---Intermittent Injection (Jul 25, 1989)

Source page: https://510kreport.com/company/medi-dose-group