Clearance Summary
PROGEL(TM), MODELS 8630 AND 8635 received FDA 510(k) clearance under submission number K882887, sponsored by Medical Devices, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1988-09-29.
- Submission: K882887
- Applicant / Sponsor: Medical Devices, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1320
- Decision date: 1988-09-29
Classification & Regulation
This clearance is catalogued under FDA product code GXY and 21 CFR 882.1320, within the Neurology review panel as a Class II device.