510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K952284Substantially Equivalent

Amerlite Tbg Assay

Johnson & Johnson Clinical Diagnostics, Inc., Rochester NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K952284 is the FDA 510(k) clearance record for AMERLITE TBG ASSAY, a class II device, cleared for Johnson & Johnson Clinical Diagnostics, Inc. on under FDA product code CEE (Radioimmunoassay, Thyroxine-Binding Globulin). FDA records list 33 510(k) clearances for Johnson & Johnson Clinical Diagnostics, Inc., from to . As of , FDA records show no recalls naming K952284.

Clearance record

Decision date
Received
(71 days to decision)
Product code
CEE Radioimmunoassay, Thyroxine-Binding Globulin
Regulation
21 CFR 862.1685
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Johnson & Johnson Clinical Diagnostics, Inc. 100 Indigo Creek Dr., Rochester NY
510(k) summary
Statement
Third party review
No

Clearances, product code CEE

Trailing 12 months

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

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