Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K030532
Device Classification Name
Device, Counter-Pulsating, External
More FDA Info for this Device
510(K) Number
K030532
Device Name
Device, Counter-Pulsating, External
Applicant
CPCA2000 INC
6336 17TH ST. CIRCLE EAST
SARASOTA, FL 34243 US
Other 510(k) Applications for this Company
Contact
ROD SHIPMAN
Other 510(k) Applications for this Contact
Regulation Number
870.5225
More FDA Info for this Regulation Number
Classification Product Code
DRN
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/19/2003
Decision Date
03/14/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact