Clearance Summary
Adscope 658 Electronic Stethoscope received FDA 510(k) clearance under submission number K162589, sponsored by American Diagnostic Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2017-03-10.
- Submission: K162589
- Applicant / Sponsor: American Diagnostic Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1875
- Decision date: 2017-03-10
Classification & Regulation
This clearance is catalogued under FDA product code DQD and 21 CFR 870.1875, within the Cardiovascular review panel as a Class II device.