Clearance Summary
ADAC MODEL ARC-5000, GAMMA CAMERA received FDA 510(k) clearance under submission number K873075, sponsored by Adac Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1987-10-30.
- Submission: K873075
- Applicant / Sponsor: Adac Laboratories
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1310
- Decision date: 1987-10-30
Classification & Regulation
This clearance is catalogued under FDA product code JWM and 21 CFR 892.1310, within the Radiology review panel as a Class II device.