510(k) K081718

EXPRESS CHEST DRAIN by Atrium Medical Corp. — Product Code KDQ

K081718 is an FDA 510(k) premarket notification submitted by Atrium Medical Corp. for the device "EXPRESS CHEST DRAIN". The FDA issued a decision of Substantially Equivalent on July 25, 2008. The device falls under product code KDQ (Bottle, Collection, Vacuum), a Class II device regulated under 21 CFR 880.6740. Atrium Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 25, 2008
Date Received
June 18, 2008
Clearance Type
Special
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