Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by Robert E Kaplan
FDA 510(k) Number
Submission Date
Device Name
Applicant
K151922
07/13/2015
StimSox(TM) System
StimMed, LLC
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact