Clearance Summary
KONIX STERILE GEL received FDA 510(k) clearance under submission number K130581, sponsored by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasa. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2014-06-18.
- Submission: K130581
- Applicant / Sponsor: Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasa
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1570
- Decision date: 2014-06-18
Classification & Regulation
This clearance is catalogued under FDA product code MUI and 21 CFR 892.1570, within the Radiology review panel as a Class II device.