Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K192252
Device Classification Name
Massager, Powered Inflatable Tube
More FDA Info for this Device
510(K) Number
K192252
Device Name
Massager, Powered Inflatable Tube
Applicant
Menlo Brands LLC
2045 Avy Avenue
Menlo Park, CA 94025 US
Other 510(k) Applications for this Company
Contact
Sam Chi
Other 510(k) Applications for this Contact
Regulation Number
890.5650
More FDA Info for this Regulation Number
Classification Product Code
IRP
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/20/2019
Decision Date
09/19/2019
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
Y
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact