Steripak, Ltd.

Steripak, Ltd. holds 2 FDA 510(k) medical device clearances, cleared in 1998.

Top product codes for Steripak, Ltd.

CAF — Anesthesiology1 device
FRO — Unknown1 device

Recent clearances by Steripak, Ltd.

K980829 — 3ML STERI-NEB SALINE - 0.9% W/V SODIUM CHLORIDE INHALATION SOLUTION USPCode CAF·1998-06-02
K972185 — 20 ML NORMAL SALINE TOPICAL SOLUTION, 0.9% W/V SODIUM CHLORIDECode FRO·1998-03-05

Data sourced from openFDA. This site is unofficial and independent of the FDA.