510(k) K896697

PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI by Deknatel, Inc. — Product Code KDQ

K896697 is an FDA 510(k) premarket notification submitted by Deknatel, Inc. for the device "PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI". The FDA issued a decision of Substantially Equivalent on February 8, 1990. 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
February 8, 1990
Date Received
November 28, 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