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

BEAR and BEAR mini

K Number: K200803 · Decision Jul 31, 2020
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
77
Applicant Total
10
Review Days
126

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Basic Information

Device Name
BEAR and BEAR mini
K Number
K200803
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Foreo, Inc.
Date Received
March 27, 2020
Decision Date
July 31, 2020
Product Code
NFO
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes

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