Clearance Summary
VACUSHIELD TM received FDA 510(k) clearance under submission number K813159, sponsored by Gelman Sciences, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1981-12-08.
- Submission: K813159
- Applicant / Sponsor: Gelman Sciences, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2050
- Decision date: 1981-12-08
Classification & Regulation
This clearance is catalogued under FDA product code JRL and 21 CFR 862.2050, within the Clinical Chemistry review panel as a Class I device.