Medical Device Manufacturer · US , Walker , MI

Meridian Diagnostics, Inc. - FDA 510(k) Cleared Devices

92 submissions · 92 cleared · Since 1980

92

Total

92

Cleared

0

Denied

FDA 510(k) Regulatory Record - Meridian Diagnostics, Inc. Pathology ✕

8 devices

1-8 of 8

Cleared Nov 10, 1981

NEUTRAL DUFFERED FORMA-SCENT

Pathology · 34d

Cleared Nov 12, 1980

PLEASCENT OR FORMA-SCENT

Pathology · 28d

Cleared Jan 24, 1980

Pathology · 28d

Cleared Jan 24, 1980

PARA-PAK(WHEATLEY'S TRICHROME STAIN)

Pathology · 28d

Cleared Jan 24, 1980

KOH MOUNTING FLUID W/GLYCEROL

Pathology · 28d

Cleared Jan 24, 1980

Pathology · 28d

Cleared Jan 21, 1980

PARA-PAK FORMALIN

Pathology · 25d

Cleared Jan 21, 1980

Pathology · 25d