Clearance Summary
9100 DAYSTAR AND 9110 ORBITER PACKAGE received FDA 510(k) clearance under submission number K781887, sponsored by Castle Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1978-12-12.
- Submission: K781887
- Applicant / Sponsor: Castle Co.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4580
- Decision date: 1978-12-12
Classification & Regulation
This clearance is catalogued under FDA product code FSY and 21 CFR 878.4580, within the General, Plastic Surgery review panel as a Class II device.