Clearance Summary
FIRSTSAVE BIPHASIC MODEL #9200 AND 9210 received FDA 510(k) clearance under submission number K010214, sponsored by Survivalink Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2001-02-22.
- Submission: K010214
- Applicant / Sponsor: Survivalink Corp.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class III
- Regulation citation: 21 CFR 870.5310
- Decision date: 2001-02-22
Classification & Regulation
This clearance is catalogued under FDA product code MKJ and 21 CFR 870.5310, within the Cardiovascular review panel as a Class III device.