Clearance Summary
PERCUSSIVENEB, MODEL PN-2001 received FDA 510(k) clearance under submission number K003684, sponsored by Vortran Medical Technology 1, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2001-02-23.
- Submission: K003684
- Applicant / Sponsor: Vortran Medical Technology 1, Inc.
- Clearance pathway: Special
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5905
- Decision date: 2001-02-23
Classification & Regulation
This clearance is catalogued under FDA product code NHJ and 21 CFR 868.5905, within the Anesthesiology review panel as a Class II device.