510(k) K892915

PLEUR-EVAC A-8002--ADULT/PEDIATRIC DUAL COLLECTION by Deknatel, Inc. — Product Code KDQ

K892915 is an FDA 510(k) premarket notification submitted by Deknatel, Inc. for the device "PLEUR-EVAC A-8002--ADULT/PEDIATRIC DUAL COLLECTION". The FDA issued a decision of Substantially Equivalent on June 21, 1989. 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
June 21, 1989
Date Received
April 20, 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