Clearance Summary
AIRSTRIP RPM FOR LIFENET CONSULT received FDA 510(k) clearance under submission number K121712, sponsored by Airstrip Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-11-20.
- Submission: K121712
- Applicant / Sponsor: Airstrip Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2300
- Decision date: 2012-11-20
Classification & Regulation
This clearance is catalogued under FDA product code MSX and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.