510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K022660Substantially Equivalent

Biocheck Myoglobin Elisa, Model Bc-1117

BioCheck Inc, Northridge CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K022660 is the FDA 510(k) clearance record for BIOCHECK MYOGLOBIN ELISA, MODEL BC-1117, a class II device, cleared for Biocheck, Inc. on under FDA product code DRR (Amplifier And Signal Conditioner, Biopotential). FDA records list 14 510(k) clearances for Biocheck, Inc., from to . As of , FDA records show no recalls naming K022660.

Clearance record

Decision date
Received
(132 days to decision)
Product code
DRR Amplifier And Signal Conditioner, Biopotential
Regulation
21 CFR 870.2050
Device class
Class II
Review panel
Cardiovascular
Applicant
Biocheck, Inc. 9418 Lasaine Ave., Northridge CA
510(k) summary
Statement
Third party review
No

Clearances, product code DRR

Trailing 12 months

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

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