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

ARIA WIFI SMART SCALE

K Number: K133872 · Decision Jun 2, 2014
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
78
Applicant Total
3
Review Days
164

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ARIA WIFI SMART SCALE
K Number
K133872
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2770
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fitbit, Inc.
Date Received
December 20, 2013
Decision Date
June 2, 2014
Product Code
MNW
Advisory Committee
Cardiovascular
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
MNW Analyzer, Body Composition

Similar 510(k) Clearances

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

View all

Other Clearances by Fitbit, Inc.

K Number Device Name
K212372 Fitbit Irregular Rhythm Notifications
K200948 Fitbit ECG App