510(k) Report

FDA applicant

Shargh Pharmaceutical Co., Inc.

Culver City, CA5 decisions1990–20020 recalls

FDA records 5 decisions for Shargh Pharmaceutical Co., Inc. (Culver City, CA) from 1990 to 2002: 5 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and FMI (Needle, Hypodermic, Single Lumen). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Shargh Pharmaceutical Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Shargh Pharmaceutical Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Shargh Pharmaceutical Co., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • FMFSyringe, Piston2decisions
  • FMINeedle, Hypodermic, Single Lumen1decision
  • FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days1decision
  • FIENeedle, Fistula1decision

What has FDA decided for it lately?

  • K013384Sharghp a.V. Fistula Needle SetShargh Pharmaceutical Co., Inc. · 2002
  • K895980Sharghp Insulin SyringesShargh Pharmaceutical Co., Inc. · 1990
  • K895811Sharghp Hypodermic NeedleShargh Pharmaceutical Co., Inc. · 1990
  • K895810Sharghp Syringes, with and Without NeedleShargh Pharmaceutical Co., Inc. · 1990
  • K895812Sharghp Intravenous CatheterShargh Pharmaceutical Co., Inc. · 1990

All 5 as Shargh Pharmaceutical Co., Inc. →