510(k) K092148

HAMILTON-C2 by Hamilton Medical AG — Product Code CBK

K092148 is an FDA 510(k) premarket notification submitted by Hamilton Medical AG for the device "HAMILTON-C2". The FDA issued a decision of Substantially Equivalent on March 4, 2010. The device falls under product code CBK (Ventilator, Continuous, Facility Use), a Class II device regulated under 21 CFR 868.5895. Hamilton Medical AG has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 4, 2010
Date Received
July 15, 2009
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ventilator, Continuous, Facility Use
Device Class
Class II
Regulation Number
868.5895
Review Panel
AN
Submission Type