Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K070336
Device Classification Name
Generator, Lesion, Radiofrequency
More FDA Info for this Device
510(K) Number
K070336
Device Name
Generator, Lesion, Radiofrequency
Applicant
STOCKERT GMBH
BOETZINGER STRASSE 72
FREIBURG, B-W D-79111 DE
Other 510(k) Applications for this Company
Contact
DOMINIKA SCHULER
Other 510(k) Applications for this Contact
Regulation Number
882.4400
More FDA Info for this Regulation Number
Classification Product Code
GXD
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/05/2007
Decision Date
06/14/2007
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