510(k) K897125

ATRIUM 2000, CHEST DRAIN by Atrium Medical Corp. — Product Code KDQ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 30, 1990
Date Received
December 26, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bottle, Collection, Vacuum
Device Class
Class II
Regulation Number
880.6740
Review Panel
HO
Submission Type