510(k) K882223

PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST by Deknatel, Inc. — Product Code KDQ

K882223 is an FDA 510(k) premarket notification submitted by Deknatel, Inc. for the device "PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST". The FDA issued a decision of Substantially Equivalent on August 16, 1988. The device falls under product code KDQ (Bottle, Collection, Vacuum), a Class II device regulated under 21 CFR 880.6740. Deknatel, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 16, 1988
Date Received
May 26, 1988
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