Clearance Summary
INTERCEPT ORAL FLUID DRUG TEST ORAL SPECIMEN COLLECTION DEVICE, MODEL 503-XXXX received FDA 510(k) clearance under submission number K011057, sponsored by OraSure Technologies, 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 2001-06-06.
- Submission: K011057
- Applicant / Sponsor: OraSure Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1675
- Decision date: 2001-06-06
Classification & Regulation
This clearance is catalogued under FDA product code PJD and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.