Clearance Summary
AP-1 AUTO PROGRAMMER received FDA 510(k) clearance under submission number K792590, sponsored by Burdick Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1980-01-04.
- Submission: K792590
- Applicant / Sponsor: Burdick Corp.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5380
- Decision date: 1980-01-04
Classification & Regulation
This clearance is catalogued under FDA product code IOL and 21 CFR 890.5380, within the Physical Medicine review panel as a Class I device.