Clearance Summary
SOLAR SPECS received FDA 510(k) clearance under submission number K970759, sponsored by Morris Rosenbloom & Co., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1997-05-06.
- Submission: K970759
- Applicant / Sponsor: Morris Rosenbloom & Co., Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.5850
- Decision date: 1997-05-06
Classification & Regulation
This clearance is catalogued under FDA product code HQY and 21 CFR 886.5850, within the Ophthalmic review panel as a Class I device.