510(k) K172803
K172803 is an FDA 510(k) premarket notification submitted by Infinitt Healthcare Co., Ltd. for the device "Infinitt PACS 7.0". The FDA issued a decision of Substantially Equivalent on October 27, 2017. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Infinitt Healthcare Co., Ltd. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 27, 2017
- Date Received
- September 18, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Image Processing, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2050
- Review Panel
- RA
- Submission Type