510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K002450Substantially Equivalent

Genua Menopause Monitor Test Kit

Genua 1944, Inc., Blairstown NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002450 is the FDA 510(k) clearance record for GENUA MENOPAUSE MONITOR TEST KIT, a class I device, cleared for Genua 1944, Inc. on under FDA product code CGJ (Radioimmunoassay, Follicle-Stimulating Hormone). FDA records list one 510(k) clearance for Genua 1944, Inc. As of , FDA records show no recalls naming K002450.

Clearance record

Decision date
Received
(156 days to decision)
Product code
CGJ Radioimmunoassay, Follicle-Stimulating Hormone
Regulation
21 CFR 862.1300
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Genua 1944, Inc. 53 Cedar Lake Rd., Blairstown NJ
510(k) summary
Statement
Third party review
No

Clearances, product code CGJ

Trailing 12 months

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

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