510(k) K023729
K023729 is an FDA 510(k) premarket notification submitted by Astron Clinica Limited for the device "SIASCOPE II". The FDA issued a decision of Substantially Equivalent on February 3, 2003. The device falls under product code PSN (Light Based Imaging), a Class II device regulated under 21 CFR 878.4580. Astron Clinica Limited has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 3, 2003
- Date Received
- November 6, 2002
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Light Based Imaging
- Device Class
- Class II
- Regulation Number
- 878.4580
- Review Panel
- SU
- Submission Type
Emission and collection of light to create an image for medical purposes