Clearance Summary
ROCHESTER MEDICAL CORPORATION SILICONE MALE EXTERNAL CATHETER received FDA 510(k) clearance under submission number K952082, sponsored by Rochester Medical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1995-07-18.
- Submission: K952082
- Applicant / Sponsor: Rochester Medical Corp.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.5250
- Decision date: 1995-07-18
Classification & Regulation
This clearance is catalogued under FDA product code EXJ and 21 CFR 876.5250, within the Gastroenterology, Urology review panel as a Class I device.