Clearance Summary
VM PLUS PEAK FLOWMETER received FDA 510(k) clearance under submission number K962074, sponsored by Clement Clarke Intl., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1997-01-02.
- Submission: K962074
- Applicant / Sponsor: Clement Clarke Intl., Ltd.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.1860
- Decision date: 1997-01-02
Classification & Regulation
This clearance is catalogued under FDA product code BZH and 21 CFR 868.1860, within the Anesthesiology review panel as a Class II device.