Medical Device Manufacturer · GB , Bedford Mk41 Oqg

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

73 submissions · 73 cleared · Since 1986

73

Total

73

Cleared

0

Denied

FDA 510(k) Regulatory Record - Unipath , Ltd. Toxicology ✕

1 devices

1-1 of 1

Cleared Nov 10, 1988

TURBOX THEOPHYLLINE ASSAY

Toxicology · 141d