FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PHILIPS ECG LEADWIRE SET

K Number: K110287 · Decision Feb 15, 2011
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
104
Applicant Total
107
Review Days
15

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Basic Information

Device Name
PHILIPS ECG LEADWIRE SET
K Number
K110287
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
870.2900
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Philips Medical Systems
Date Received
January 31, 2011
Decision Date
February 15, 2011
Product Code
DSA
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DSA Cable, Transducer And Electrode, Patient, (Including Connector)

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