510(k) K952597
K952597 is an FDA 510(k) premarket notification submitted by Point of View Optical Outlet, Inc. for the device "VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW". The FDA issued a decision of Substantially Equivalent on September 12, 1995. The device falls under product code HQZ (Frame, Spectacle), a Class I device regulated under 21 CFR 886.5842.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 12, 1995
- Date Received
- June 6, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Frame, Spectacle
- Device Class
- Class I
- Regulation Number
- 886.5842
- Review Panel
- OP
- Submission Type