Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K993202
Device Classification Name
Device, Galvanic Skin Response Measurement
More FDA Info for this Device
510(K) Number
K993202
Device Name
Device, Galvanic Skin Response Measurement
Applicant
GENERAL DEVICES
1000 RIVER ST.
RIDGEFIELD, NJ 07657 US
Other 510(k) Applications for this Company
Contact
MICHAEL SMITH
Other 510(k) Applications for this Contact
Regulation Number
882.1540
More FDA Info for this Regulation Number
Classification Product Code
GZO
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/24/1999
Decision Date
12/17/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact