510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K123567Substantially Equivalent

First Response Gold Digital Pregnancy Test

Church & Dwight Co., Inc., Princeton NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K123567 is the FDA 510(k) clearance record for FIRST RESPONSE GOLD DIGITAL PREGNANCY TEST, a class II device, cleared for Church & Dwight Co., Inc. on under FDA product code LCX (Kit, Test, Pregnancy, Hcg, Over The Counter). FDA records list 29 510(k) clearances for Church & Dwight Co., Inc., from to . As of , FDA records show no recalls naming K123567.

Clearance record

Decision date
Received
(294 days to decision)
Product code
LCX Kit, Test, Pregnancy, Hcg, Over The Counter
Regulation
21 CFR 862.1155
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Church & Dwight Co., Inc. 469 N. Harrison St., Princeton NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LCX

Trailing 12 months

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

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