# Hirata Sangyo Co. USA, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 8 (1982–1986): 8 510(k) clearances
- Product codes: FRN (3), DXN (2), HTO (1), GEN (1), GAD (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
- K864106: SR-Model 230 (Modification) (Nov 19, 1986)
- K842289: SR- Model 230 (Jul 25, 1984)
- K833542: Surgical Instrument (Nov 28, 1983)
- K833541: Surgical Instrument (Nov 28, 1983)
- K832686: Multiple Manual Surgical Instruments (Oct 14, 1983)
- K831583: GP-303 (Jul 19, 1983)
- K821989: Non-Stetho 7, UM-15TP (Oct 18, 1982)
- K822571: Syringe Pump (Oct 8, 1982)

Source page: https://510kreport.com/company/hirata-sangyo-co-usa