510(k) K182926
K182926 is an FDA 510(k) premarket notification submitted by Philips Healthcare Informatics, Inc. for the device "IntelliSpace Radiology". The FDA issued a decision of Substantially Equivalent on December 6, 2018. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Philips Healthcare Informatics, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 6, 2018
- Date Received
- October 22, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- System, Image Processing, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2050
- Review Panel
- RA
- Submission Type