Clearance Summary
STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS received FDA 510(k) clearance under submission number K990512, sponsored by Stoeckert Instrumente. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1999-11-23.
- Submission: K990512
- Applicant / Sponsor: Stoeckert Instrumente
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class I
- Regulation citation: 21 CFR 870.4200
- Decision date: 1999-11-23
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.