Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K170667
Device Classification Name
Endoscope, Neurological
More FDA Info for this Device
510(K) Number
K170667
Device Name
Endoscope, Neurological
Applicant
Carl Zeiss Meditec AG
Goeschwitzer Strasse 51-52
Jena 07745 DE
Other 510(k) Applications for this Company
Contact
Christian Muenster
Other 510(k) Applications for this Contact
Regulation Number
882.1480
More FDA Info for this Regulation Number
Classification Product Code
GWG
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/06/2017
Decision Date
08/18/2017
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact