510(k) K211901
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 21, 2021
- Date Received
- June 21, 2021
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Autofluorescence Imaging Adjunct Tool For Wounds
- Device Class
- Class II
- Regulation Number
- 878.4550
- Review Panel
- SU
- Submission Type
An autofluorescence detection device for general surgery and dermatological use is an adjunct tool that uses autofluorescence to detect tissues or structures. This device is not intended to provide a diagnosis.