Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K020660
Device Classification Name
Pump, Infusion, Elastomeric
More FDA Info for this Device
510(K) Number
K020660
Device Name
Pump, Infusion, Elastomeric
Applicant
I-FLOW CORP.
20202 WINDROW DR.
LAKE FOREST, CA 92630 US
Other 510(k) Applications for this Company
Contact
SHANE NOEHRE
Other 510(k) Applications for this Contact
Regulation Number
880.5725
More FDA Info for this Regulation Number
Classification Product Code
MEB
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/01/2002
Decision Date
03/20/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact