510(k) K203087
K203087 is an FDA 510(k) premarket notification submitted by Philips Medical Systems Dmc GmbH for the device "CombiDiagnost R90". The FDA issued a decision of Substantially Equivalent on December 3, 2020. The device falls under product code JAA (System, X-Ray, Fluoroscopic, Image-Intensified), a Class II device regulated under 21 CFR 892.1650. Philips Medical Systems Dmc GmbH has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 3, 2020
- Date Received
- October 13, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- System, X-Ray, Fluoroscopic, Image-Intensified
- Device Class
- Class II
- Regulation Number
- 892.1650
- Review Panel
- RA
- Submission Type