510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K921012Substantially Equivalent

Precise Chromatographic Immunoassay for Hcg

BD Becton Dickinson Vacutainer Systems Preanalytic, Cockeysville MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K921012 is the FDA 510(k) clearance record for PRECISE CHROMATOGRAPHIC IMMUNOASSAY FOR HCG, a class II device, cleared for Bd Becton Dickinson Vacutainer Systems Preanalytic on under FDA product code LCX (Kit, Test, Pregnancy, Hcg, Over The Counter). FDA records list 632 510(k) clearances for Bd Becton Dickinson Vacutainer Systems Preanalytic, from to . As of , FDA records show no recalls naming K921012.

Clearance record

Decision date
Received
(36 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
Bd Becton Dickinson Vacutainer Systems Preanalytic P.O. Box 243, Cockeysville MD
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 November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LCX, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260