510(k) K151097

Active Breathing Coordinator by Aktina Medical Corporation — Product Code IYE

K151097 is an FDA 510(k) premarket notification submitted by Aktina Medical Corporation for the device "Active Breathing Coordinator". The FDA issued a decision of Substantially Equivalent on May 15, 2015. The device falls under product code IYE (Accelerator, Linear, Medical), a Class II device regulated under 21 CFR 892.5050. Aktina Medical Corporation has 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 15, 2015
Date Received
Apr 24, 2015
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Accelerator, Linear, Medical
Device Class
Class II
Regulation Number
892.5050
Review Panel
RA
Submission Type
510(k)