Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K020468
Device Classification Name
Electrode, Cutaneous
More FDA Info for this Device
510(K) Number
K020468
Device Name
Electrode, Cutaneous
Applicant
DYMEDIX, INC.
800 LEVANGER LN.
STOUGHTON, WI 53589 US
Other 510(k) Applications for this Company
Contact
Gary Syring
Other 510(k) Applications for this Contact
Regulation Number
882.1320
More FDA Info for this Regulation Number
Classification Product Code
GXY
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/12/2002
Decision Date
04/16/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact