510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K920318Substantially Equivalent

Cedia Ferritin Assay

Microgenics Corporation, Concord CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K920318 is the FDA 510(k) clearance record for CEDIA FERRITIN ASSAY, a class II device, cleared for Microgenics Corp. on under FDA product code JMG (Radioimmunoassay (Two-Site Solid Phase), Ferritin). FDA records list 128 510(k) clearances for Microgenics Corp., from to . As of , FDA records show no recalls naming K920318.

Clearance record

Decision date
Received
(132 days to decision)
Product code
JMG Radioimmunoassay (Two-Site Solid Phase), Ferritin
Regulation
21 CFR 866.5340
Device class
Class II
Review panel
Immunology
Applicant
Microgenics Corp. 2380a Bisso Ln., Concord CA
510(k) summary
Statement
Third party review
No

Clearances, product code JMG

Trailing 12 months

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

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