Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K993088
Device Classification Name
Generator, Oxygen, Portable
More FDA Info for this Device
510(K) Number
K993088
Device Name
Generator, Oxygen, Portable
Applicant
PURITAN BENNETT CORP.
2200 FARADAY AVE.
CARLSBAD, CA 92008 US
Other 510(k) Applications for this Company
Contact
TONY KEAVENEY
Other 510(k) Applications for this Contact
Regulation Number
868.5440
More FDA Info for this Regulation Number
Classification Product Code
CAW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/16/1999
Decision Date
10/08/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact