Clearance Summary
ROYAL FLASH received FDA 510(k) clearance under submission number K952939, sponsored by Royal Flash Enterprise Co. , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1995-08-07.
- Submission: K952939
- Applicant / Sponsor: Royal Flash Enterprise Co. , Ltd.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.5850
- Decision date: 1995-08-07
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.