510(k) K201081
K201081 is an FDA 510(k) premarket notification submitted by Philips Medical System Nederland B.V. for the device "AltaTrack equipment, AltaTrack Guidewire, AltaTrack Catheter". The FDA issued a decision of Substantially Equivalent on Dec 17, 2020. The device falls under product code DQK (Computer, Diagnostic, Programmable), a Class II device regulated under 21 CFR 870.1425.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 17, 2020
- Date Received
- Apr 22, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Computer, Diagnostic, Programmable
- Device Class
- Class II
- Regulation Number
- 870.1425
- Review Panel
- CV
- Submission Type
- 510(k)