Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K983610
Device Classification Name
Filter, Bacterial, Breathing-Circuit
More FDA Info for this Device
510(K) Number
K983610
Device Name
Filter, Bacterial, Breathing-Circuit
Applicant
INTERSURGICAL, INC.
417 ELECTRONICS PKWY.
LIVERPOOL, NY 13088 US
Other 510(k) Applications for this Company
Contact
THOMAS R GUNERMAN
Other 510(k) Applications for this Contact
Regulation Number
868.5260
More FDA Info for this Regulation Number
Classification Product Code
CAH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/14/1998
Decision Date
04/30/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact