510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K912408Substantially Equivalent

Merifluor-Cryptosporidium/giardia

Meridian Diagnostics, Inc., Cincinnati OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K912408 is the FDA 510(k) clearance record for MERIFLUOR-CRYPTOSPORIDIUM/GIARDIA, a class II device, cleared for Meridian Diagnostics, Inc. on under FDA product code MHI (Giardia Spp.). FDA records list 92 510(k) clearances for Meridian Diagnostics, Inc., from to . As of , FDA records show no recalls naming K912408.

Clearance record

Decision date
Received
(54 days to decision)
Product code
MHI Giardia Spp.
Regulation
21 CFR 866.3220
Device class
Class II
Review panel
Microbiology
Applicant
Meridian Diagnostics, Inc. 3471 River Hills Dr., Cincinnati OH
510(k) summary
Statement
Third party review
No

Clearances, product code MHI

Trailing 12 months

FDA records hold no clearances under product code MHI in the trailing twelve months.

FDA records show no clearances under product code MHI in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MHI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260