Clearance Summary
STETHOSCOPE received FDA 510(k) clearance under submission number K904547, sponsored by Kimball Industries Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1991-03-21.
- Submission: K904547
- Applicant / Sponsor: Kimball Industries Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class I
- Regulation citation: 21 CFR 870.1875
- Decision date: 1991-03-21
Classification & Regulation
This clearance is catalogued under FDA product code LDE and 21 CFR 870.1875, within the Cardiovascular review panel as a Class I device.