# Lyphomed, Inc.

- Location (FDA's records): Melrose Park, IL
- FDA decisions: 8 (1984–1991): 8 510(k) clearances
- Product codes: FPA (5), LHI (2)
- 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
- K910142: Spark Kit (R), Modification (May 14, 1991)
- K864509: Spark-Kit (TM) (Feb 18, 1987)
- K853019: Nitroglycerin Infusion Set (Nov 12, 1985)
- K853086: Secondary Administration Set (Aug 19, 1985)
- K852882: Maxifill Transfer Set (Aug 16, 1985)
- K852881: Vented Secondary IV Administration Set (Aug 16, 1985)
- K842678: I.V. Transfer Spike (Oct 9, 1984)
- K842345: Maxifill Transfer Set (Aug 17, 1984)

Source page: https://510kreport.com/company/lyphomed