Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K983926
Device Classification Name
Set, Administration, Intravascular
More FDA Info for this Device
510(K) Number
K983926
Device Name
Set, Administration, Intravascular
Applicant
CRITICAL DEVICE CORP.
499 NIBUS ST.
BREA, CA 92621 US
Other 510(k) Applications for this Company
Contact
DAN HYUN
Other 510(k) Applications for this Contact
Regulation Number
880.5440
More FDA Info for this Regulation Number
Classification Product Code
FPA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/05/1998
Decision Date
01/20/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact