Duns Number:631535262
Device Description: PYLARIFY AI is a software only medical device that provides quantitative assessments of st PYLARIFY AI is a software only medical device that provides quantitative assessments of standardized uptake values (SUVs) for patients that are subject to examination by nuclear medicine (NM) imaging, using PSMA PET/CT, within the clinical application of oncology. The device performs by automatic organ and bone segmentation and lesions, selected by the user, will automatically be calculated into a lesion index (LI) and intensity-weighted total lesion volume (ITLV). The user of this product is typically a health-care professional using the software to review patient images and analyze results.
Catalog Number
601
Brand Name
PYLARIFY AI
Version/Model Number
01
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 26, 2022
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K211655
Product Code
LLZ
Product Code Name
System, Image Processing, Radiological
Public Device Record Key
0c9fbd5e-8644-489a-bfd9-6344efb5c081
Public Version Date
August 29, 2022
Public Version Number
2
DI Record Publish Date
November 16, 2021
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 5 |