510(k) K940886

ANNELID by Kinetic Concepts, Inc. — Product Code JCX

K940886 is an FDA 510(k) premarket notification submitted by Kinetic Concepts, Inc. for the device "ANNELID". The FDA issued a decision of Substantially Equivalent on November 17, 1994. The device falls under product code JCX (Apparatus, Suction, Ward Use, Portable, Ac-Powered), a Class II device regulated under 21 CFR 878.4780. Kinetic Concepts, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 17, 1994
Date Received
February 25, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Apparatus, Suction, Ward Use, Portable, Ac-Powered
Device Class
Class II
Regulation Number
878.4780
Review Panel
SU
Submission Type