Medical Device Manufacturer · GB , Runcorn, Cheshire

Steripak, Ltd. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 1998

Recent clearances: 20 ML NORMAL SALINE TOPICAL SOLUTION, 0.9% W/V SODIUM CHLORIDE

2

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Steripak, Ltd. Anesthesiology ✕

1 devices

1-1 of 1

Cleared Jun 02, 1998

3ML STERI-NEB SALINE - 0.9% W/V SODIUM CHLORIDE INHALATION SOLUTION USP

Anesthesiology · 90d