Clearance Summary
INTERFACE MODULE IDDD received FDA 510(k) clearance under submission number K992635, sponsored by Stoeckert Instrumente. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1999-12-20.
- Submission: K992635
- Applicant / Sponsor: Stoeckert Instrumente
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class I
- Regulation citation: 21 CFR 870.4200
- Decision date: 1999-12-20
Classification & Regulation
This clearance is catalogued under FDA product code KRI and 21 CFR 870.4200, within the Cardiovascular review panel as a Class I device.