510(k) K173433
K173433 is an FDA 510(k) premarket notification submitted by Philips Medical Systems Dmc GmbH for the device "ProxiDiagnost N90". The FDA issued a decision of Substantially Equivalent on Feb 5, 2018. The device falls under product code OWB (Interventional Fluoroscopic X-Ray System), a Class II device regulated under 21 CFR 892.1650. Philips Medical Systems Dmc GmbH has 17 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 5, 2018
- Date Received
- Nov 2, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Interventional Fluoroscopic X-Ray System
- Device Class
- Class II
- Regulation Number
- 892.1650
- Review Panel
- RA
- Submission Type
- 510(k)
Interventional fluoroscopy