Clearance Summary
FAST TRACT TRANSTRACHEAL PROCEDURE KIT received FDA 510(k) clearance under submission number K970018, sponsored by L.W. Ward and Assoc., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1997-03-28.
- Submission: K970018
- Applicant / Sponsor: L.W. Ward and Assoc., Inc.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.4420
- Decision date: 1997-03-28
Classification & Regulation
This clearance is catalogued under FDA product code LRC and 21 CFR 874.4420, within the Ear, Nose, Throat review panel as a Class I device.