# Shargh Pharmaceutical Co., Inc.

- Location (FDA's records): Culver City, CA
- FDA decisions: 5 (1990–2002): 5 510(k) clearances
- Product codes: FMF (2), FMI (1), FOZ (1), FIE (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
- K013384: Sharghp a.V. Fistula Needle Set (Jan 7, 2002)
- K895980: Sharghp Insulin Syringes (Sep 7, 1990)
- K895811: Sharghp Hypodermic Needle (Sep 7, 1990)
- K895810: Sharghp Syringes, with and Without Needle (Sep 7, 1990)
- K895812: Sharghp Intravenous Catheter (Sep 7, 1990)

Source page: https://510kreport.com/company/shargh-pharmaceutical