510(k) K131313
K131313 is an FDA 510(k) premarket notification submitted by Aktina Medical Corp. for the device "ACTIVE BREATHING COORDINATOR". The FDA issued a decision of Substantially Equivalent on Aug 7, 2013. The device falls under product code IYE (Accelerator, Linear, Medical), a Class II device regulated under 21 CFR 892.5050.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 7, 2013
- Date Received
- May 7, 2013
- Clearance Type
- Traditional
- 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)