510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K033155Substantially Equivalent

Biocentrex Cardiac Panel

Biocentrex, Culver City CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K033155 is the FDA 510(k) clearance record for BIOCENTREX CARDIAC PANEL, a class II device, cleared for Biocentrex on under FDA product code MYT (Biosensor, Immunoassay, Cpk Or Isoenzymes). FDA records list one 510(k) clearance for Biocentrex. As of , FDA records show no recalls naming K033155.

Clearance record

Decision date
Received
(104 days to decision)
Product code
MYT Biosensor, Immunoassay, Cpk Or Isoenzymes
Regulation
21 CFR 862.1215
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Biocentrex 6100 Bristol Pkwy., Culver City CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MYT

Trailing 12 months

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

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