510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K072732Substantially Equivalent

Ortho T. Cruzi Elisa Test System

Ortho-Clinical Diagnostics, Inc., Raritan NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072732 is the FDA 510(k) clearance record for ORTHO T. CRUZI ELISA TEST SYSTEM, a class I device, cleared for Ortho-Clinical Diagnostics, Inc. on under FDA product code MIU (Enzyme Linked Immunosorbent Assay, T. Cruzi). FDA records list 311 510(k) clearances for Ortho-Clinical Diagnostics, Inc., from to . As of , FDA records show no recalls naming K072732.

Clearance record

Decision date
Received
(567 days to decision)
Product code
MIU Enzyme Linked Immunosorbent Assay, T. Cruzi
Regulation
21 CFR 866.3870
Device class
Class I
Review panel
Microbiology
Applicant
Ortho-Clinical Diagnostics, Inc. 1001 U.S. Hwy. 202, Raritan NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MIU

Trailing 12 months

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

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