Clearance Summary
BESURE PLUS ONE-STEP HOME OVULATION PREDICTOR KIT received FDA 510(k) clearance under submission number K983113, sponsored by Syntron Bioresearch, 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 1998-11-18.
- Submission: K983113
- Applicant / Sponsor: Syntron Bioresearch, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1485
- Decision date: 1998-11-18
Classification & Regulation
This clearance is catalogued under FDA product code CEP and 21 CFR 862.1485, within the Clinical Chemistry review panel as a Class I device.