510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K020484Substantially Equivalent

Careside Ldh

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

K020484 is the FDA 510(k) clearance record for CARESIDE LDH, a class II device, cleared for Careside, Inc. on under FDA product code CFH (Tetrazolium Int Dye-Diaphorase, Lactate Dehydrogenase). FDA records list 22 510(k) clearances for Careside, Inc., from to . As of , FDA records show no recalls naming K020484.

Clearance record

Decision date
Received
(140 days to decision)
Product code
CFH Tetrazolium Int Dye-Diaphorase, Lactate Dehydrogenase
Regulation
21 CFR 862.1440
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Careside, Inc. 6100 Bristol Pkwy., Culver City CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CFH

Trailing 12 months

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

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