Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K060751
Device Classification Name
Conserver, Oxygen
More FDA Info for this Device
510(K) Number
K060751
Device Name
Conserver, Oxygen
Applicant
INOVO, INC.
2975 S. HORSESHOE DRIVE
SUITE 600
NAPLES, FL 34104 US
Other 510(k) Applications for this Company
Contact
MICHAEL T DILDINE
Other 510(k) Applications for this Contact
Regulation Number
868.5905
More FDA Info for this Regulation Number
Classification Product Code
NFB
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/21/2006
Decision Date
07/18/2006
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact