510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K972587Substantially Equivalent

Electrocardiographs

Dr. Lee Co., Ltd., Irvine CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K972587 is the FDA 510(k) clearance record for ELECTROCARDIOGRAPHS, cleared for Dr. Lee Co., Ltd. on under FDA product code LOS. FDA records list 2 510(k) clearances for Dr. Lee Co., Ltd., from to . As of , FDA records show no recalls naming K972587.

Clearance record

Decision date
Received
(406 days to decision)
Product code
LOS
Review panel
Unknown
Applicant
Dr. Lee Co., Ltd. 3722 Ave. Sausalito, Irvine CA
510(k) summary
Statement
Third party review
No

Clearances, product code LOS

Trailing 12 months

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

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