Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K992372
Device Classification Name
Cable, Electrode
More FDA Info for this Device
510(K) Number
K992372
Device Name
Cable, Electrode
Applicant
THERAPY EQUIPMENT, INC.
13860 WELLINGTON TRACE, #310
WEST PALM BEACH, FL 33414 US
Other 510(k) Applications for this Company
Contact
GLENN BUCHAN
Other 510(k) Applications for this Contact
Regulation Number
890.1175
More FDA Info for this Regulation Number
Classification Product Code
IKD
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/15/1999
Decision Date
10/13/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact