510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K073376Substantially Equivalent

Philips ECG Algorithm

Philips North America LLC, Andover MA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K073376 is the FDA 510(k) clearance record for PHILIPS ECG ALGORITHM, cleared for Philips Medical Systems on under FDA product code LOS. FDA records list 680 510(k) clearances for Philips North America LLC, from to . As of , FDA records show no recalls naming K073376.

Clearance record

Decision date
Received
(130 days to decision)
Product code
LOS
Review panel
Unknown
Applicant
Philips Medical Systems 3000 Minuteman Rd., Andover MA
510(k) summary
Summary PDF
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 November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LOS, 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