Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by gel-e, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180152
01/19/2018
gel-e Flex
gel-e, Inc.
K192667
09/25/2019
gel-e Flex+ gel OTC
gel-e, Inc.
K182811
10/03/2018
gel-e Flex+
gel-e, Inc.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact