510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K912152Substantially Equivalent

Cellabs Giardia Cel I.f. Test

Celltech Diagnostics, Ltd., Suite 11oo, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K912152 is the FDA 510(k) clearance record for CELLABS GIARDIA CEL I.F. TEST, a class II device, cleared for Celltech Diagnostics , Ltd. on under FDA product code MHI (Giardia Spp.). FDA records list one 510(k) clearance for Celltech Diagnostics , Ltd. As of , FDA records show no recalls naming K912152.

Clearance record

Decision date
Received
(89 days to decision)
Product code
MHI Giardia Spp.
Regulation
21 CFR 866.3220
Device class
Class II
Review panel
Microbiology
Applicant
Celltech Diagnostics , Ltd. C/O Baker & Hostetler, Suite 11oo, Washington DC
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