510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K832712Substantially Equivalent

Folate Radioassay Kit Ca-1562-125

Clinical Assays, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832712 is the FDA 510(k) clearance record for FOLATE RADIOASSAY KIT CA-1562-125, a class II device, cleared for Clinical Assays, Inc. on under FDA product code CGN (Acid, Folic, Radioimmunoassay). FDA records list 27 510(k) clearances for Clinical Assays, Inc., from to . As of , FDA records show no recalls naming K832712.

Clearance record

Decision date
Received
(53 days to decision)
Product code
CGN Acid, Folic, Radioimmunoassay
Regulation
21 CFR 862.1295
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Clinical Assays, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CGN

Trailing 12 months

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

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