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

Study Watch

K Number: K182456 · Decision Jan 17, 2019
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
296
Applicant Total
4
Review Days
132

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Basic Information

Device Name
Study Watch
K Number
K182456
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2920
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Verily Life Sciences, LLC
Date Received
September 7, 2018
Decision Date
January 17, 2019
Product Code
DXH
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
DXH Transmitters And Receivers, Electrocardiograph, Telephone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DXH), ordered by most recent decision date.

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Other Clearances by Verily Life Sciences, LLC

K Number Device Name
K242508 Verily Numetric Retinal Camera
K213357 Study Watch with Irregular Pulse Monitor (Home), Study Watch with Irregular Pulse Monitor
K192415 Study Watch with Irregular Pulse Monitor