Clearance Summary
ST-302 INFRAREX received FDA 510(k) clearance under submission number K990233, sponsored by Skylark Device Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1999-10-27.
- Submission: K990233
- Applicant / Sponsor: Skylark Device Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5500
- Decision date: 1999-10-27
Classification & Regulation
This clearance is catalogued under FDA product code ILY and 21 CFR 890.5500, within the Physical Medicine review panel as a Class II device.