Clearance Summary
PREAMPLIFIER MODEL 113 received FDA 510(k) clearance under submission number K781289, sponsored by Princeton Applied Research Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1978-09-14.
- Submission: K781289
- Applicant / Sponsor: Princeton Applied Research Corp.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1835
- Decision date: 1978-09-14
Classification & Regulation
This clearance is catalogued under FDA product code GWL and 21 CFR 882.1835, within the Neurology review panel as a Class II device.