Clearance Summary
AP-CHECK received FDA 510(k) clearance under submission number K830877, sponsored by General Devices. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1983-06-08.
- Submission: K830877
- Applicant / Sponsor: General Devices
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class I
- Regulation citation: 21 CFR 882.1410
- Decision date: 1983-06-08
Classification & Regulation
This clearance is catalogued under FDA product code GYA and 21 CFR 882.1410, within the Neurology review panel as a Class I device.