Meridian Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PREMIER TOXINS A&B, MODEL 616096, IMMUNOCARD STAT! E. COLI O157:H7, PREMIER TYPE SPECIFIC HSV-1 IGG ELISA TEST
92
Total
92
Cleared
0
Denied
FDA 510(k) Regulatory Record - Meridian Diagnostics, Inc. Pathology ✕
8 devices
Cleared
Nov 10, 1981
NEUTRAL DUFFERED FORMA-SCENT
Pathology
34d
Cleared
Nov 12, 1980
PLEASCENT OR FORMA-SCENT
Pathology
28d
Cleared
Jan 24, 1980
VASPAR SEALANT
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
PARA-PAK PVA
Pathology
28d
Cleared
Jan 21, 1980
PARA-PAK FORMALIN
Pathology
25d
Cleared
Jan 21, 1980
PARA-PAK SAF
Pathology
25d