Clearance Summary
TYCOS DIAGNOSTIC PENLIGHT received FDA 510(k) clearance under submission number K760972, sponsored by Taylor Instrument Analytics Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1977-01-26.
- Submission: K760972
- Applicant / Sponsor: Taylor Instrument Analytics Co.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6350
- Decision date: 1977-01-26
Classification & Regulation
This clearance is catalogued under FDA product code KYT and 21 CFR 880.6350, within the General Hospital review panel as a Class I device.