510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K912316Substantially Equivalent

Quikpac-II One Step Pregnancy Home Test

Syntron Bioresearch, Inc., Vista CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K912316 is the FDA 510(k) clearance record for QUIKPAC-II ONE STEP PREGNANCY HOME TEST, a class II device, cleared for Syntron Bioresearch, Inc. on under FDA product code LCX (Kit, Test, Pregnancy, Hcg, Over The Counter). FDA records list 26 510(k) clearances for Syntron Bioresearch, Inc., from to . As of , FDA records show no recalls naming K912316.

Clearance record

Decision date
Received
(61 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
Syntron Bioresearch, Inc. 1080 Joshua Way, Vista CA
510(k) summary
Statement
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