Clearance Summary
APOLLO DENSITOMETER received FDA 510(k) clearance under submission number K853734, sponsored by Astral Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1985-09-25.
- Submission: K853734
- Applicant / Sponsor: Astral Medical Systems
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2400
- Decision date: 1985-09-25
Classification & Regulation
This clearance is catalogued under FDA product code JQT and 21 CFR 862.2400, within the Clinical Chemistry review panel as a Class I device.