Clearance Summary
ACME GUIDEWIRES FOR PERCUTANEOUS INSERTION OF CATH received FDA 510(k) clearance under submission number K883763, sponsored by Acme-Monaco Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1988-11-18.
- Submission: K883763
- Applicant / Sponsor: Acme-Monaco Corp.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5130
- Decision date: 1988-11-18
Classification & Regulation
This clearance is catalogued under FDA product code KOD and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.