510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K110287Substantially Equivalent

Philips ECG Leadwire Set

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

K110287 is the FDA 510(k) clearance record for PHILIPS ECG LEADWIRE SET, a class II device, cleared for Philips Medical Systems on under FDA product code DSA (Cable, Transducer And Electrode, Patient, (Including Connector)). FDA records list 680 510(k) clearances for Philips North America LLC, from to . As of , FDA records show one recall naming K110287.

Clearance record

Decision date
Received
(15 days to decision)
Product code
DSA Cable, Transducer And Electrode, Patient, (Including Connector)
Regulation
21 CFR 870.2900
Device class
Class II
Review panel
Cardiovascular
Applicant
Philips Medical Systems 3000 Minuteman Rd., Andover MA
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code DSA

Trailing 12 months
2 clearances under product code DSA in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DSA, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260