510(k) K854442
K854442 is an FDA 510(k) premarket notification submitted by Optatint, Inc. for the device "UVASORB-400". The FDA issued a decision of Substantially Equivalent on February 19, 1986. The device falls under product code HPX (Lens, Contact (Polymethylmethacrylate)), a Class U device. Optatint, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 19, 1986
- Date Received
- November 5, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lens, Contact (Polymethylmethacrylate)
- Device Class
- Class U
- Regulation Number
- Review Panel
- OP
- Submission Type