510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K974111Substantially Equivalent

Quidel Ch50 Eq Eia

Ortho-Clinical Diagnostics, Inc., San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K974111 is the FDA 510(k) clearance record for QUIDEL CH50 EQ EIA, a class II device, cleared for Quidel Corp. on under FDA product code DAE (Complement C9, Antigen, Antiserum, Control). FDA records list 311 510(k) clearances for ORTHO-CLINICAL DIAGNOSTICS, INC., from to . As of , FDA records show no recalls naming K974111.

Clearance record

Decision date
Received
(271 days to decision)
Product code
DAE Complement C9, Antigen, Antiserum, Control
Regulation
21 CFR 866.5240
Device class
Class II
Review panel
Immunology
Applicant
Quidel Corp. 10165 Mckellar Ct., San Diego CA
510(k) summary
Summary
Third party review
No

Clearances, product code DAE

Trailing 12 months

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

FDA records show no clearances under product code DAE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DAE, 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