Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by RENISHAW MAYFIELD SARL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180206
01/24/2018
neuromate Gen III
Renishaw Mayfield Sarl
K181706
06/28/2018
neuromate Gen III
Renishaw Mayfield Sarl
K132755
09/03/2013
NEUROMATE FRAMELESS GEN II
RENISHAW MAYFIELD SARL
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact