510(k) K902306
K902306 is an FDA 510(k) premarket notification submitted by Vista Vision for the device "THE VISONIC DOME(TM)". The FDA issued a decision of Substantially Equivalent on December 21, 1990. The device falls under product code LYL (Accessories, Solution, Ultrasonic Cleaners For Lenses), a Class II device regulated under 21 CFR 886.5928.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 21, 1990
- Date Received
- May 22, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Accessories, Solution, Ultrasonic Cleaners For Lenses
- Device Class
- Class II
- Regulation Number
- 886.5928
- Review Panel
- OP
- Submission Type