Clearance Summary
MSA100 PEAK FLOW METER received FDA 510(k) clearance under submission number K133975, sponsored by Beijing M&B Electronic Instruments Co., 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 2014-10-03.
- Submission: K133975
- Applicant / Sponsor: Beijing M&B Electronic Instruments Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.1860
- Decision date: 2014-10-03
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.