Clearance Summary
binx health io CT/NG Assay received FDA 510(k) clearance under submission number K191352, sponsored by Binx Health, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2019-08-08.
- Submission: K191352
- Applicant / Sponsor: Binx Health, Inc.
- Clearance pathway: Traditional
- Review panel: Microbiology
- Device class: Class II
- Regulation citation: 21 CFR 866.3393
- Decision date: 2019-08-08
Classification & Regulation
This clearance is catalogued under FDA product code QEP and 21 CFR 866.3393, within the Microbiology review panel as a Class II device.