510(k) K950677

ATRIUM DRY SUCTION CONTROL WATER SEAL CHEST DRAIN by Atrium Medical Corp. — Product Code KDQ

K950677 is an FDA 510(k) premarket notification submitted by Atrium Medical Corp. for the device "ATRIUM DRY SUCTION CONTROL WATER SEAL CHEST DRAIN". The FDA issued a decision of Substantially Equivalent on April 13, 1995. 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
April 13, 1995
Date Received
February 14, 1995
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