510(k) K210512
K210512 is an FDA 510(k) premarket notification submitted by Uvision360, Inc. for the device "LUMINELLE DTx System". The FDA issued a decision of Substantially Equivalent on Jun 30, 2021. The device falls under product code FAJ (Cystoscope And Accessories, Flexible/Rigid), a Class II device regulated under 21 CFR 876.1500. Uvision360, Inc. has 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jun 30, 2021
- Date Received
- Feb 23, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cystoscope And Accessories, Flexible/Rigid
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- GU
- Submission Type
- 510(k)
To examine and perform procedures within the urinary tract. For reusable, flexible endoscopes in this product code, validated reprocessing instructions and reprocessing validation data must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).