510(k) K152899
K152899 is an FDA 510(k) premarket notification submitted by Philips Healthcare, Inc. for the device "Philips Lumify Diagnostic Ultrasound System". The FDA issued a decision of Substantially Equivalent on October 30, 2015. The device falls under product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic), a Class II device regulated under 21 CFR 892.1550.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 30, 2015
- Date Received
- October 1, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- System, Imaging, Pulsed Doppler, Ultrasonic
- Device Class
- Class II
- Regulation Number
- 892.1550
- Review Panel
- RA
- Submission Type