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

Philips Biosensor BX100

K Number: K192875 · Decision Apr 16, 2020
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
190
Applicant Total
107
Review Days
191

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Basic Information

Device Name
Philips Biosensor BX100
K Number
K192875
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2910
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Philips Medical Systems
Date Received
October 8, 2019
Decision Date
April 16, 2020
Product Code
DRG
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DRG Transmitters And Receivers, Physiological Signal, Radiofrequency

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K183387 M3290B Patient Information Center iX
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K172226 MX40 Release B.07
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