Clearance Summary
CERVINEEDLE DISPOSABLE CARTRIDGE SYRINGE received FDA 510(k) clearance under submission number K052365, sponsored by Rocket Medical Plc. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2005-10-17.
- Submission: K052365
- Applicant / Sponsor: Rocket Medical Plc
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5100
- Decision date: 2005-10-17
Classification & Regulation
This clearance is catalogued under FDA product code HEE and 21 CFR 884.5100, within the Obstetrics/Gynecology review panel as a Class II device.