FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Ambra ProViewer
K Number: K202335
·
Decision Sep 4, 2020
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
1
Review Days
18
Basic Information
- Device Name
- Ambra ProViewer
- K Number
- K202335
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.2050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Dicom Grid, Inc, dba Ambra Health
- Date Received
- August 17, 2020
- Decision Date
- September 4, 2020
- Product Code
- LLZ
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- Third Party
- Y
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LLZ | System, Image Processing, Radiological | FDA class 2 | Radiology |
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