FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

FridaMom Anti-Nausea Bands

K Number: K220289 · Decision Jun 29, 2022
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
12
Applicant Total
1
Review Days
148

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Basic Information

Device Name
FridaMom Anti-Nausea Bands
K Number
K220289
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fridababy, LLC
Date Received
February 1, 2022
Decision Date
June 29, 2022
Product Code
MVV
Advisory Committee
Unknown
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
MVV Device, Acupressure

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