Clearance Summary
LUNAPADS received FDA 510(k) clearance under submission number K010986, sponsored by Lunapads International Products, Ltd.. 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 2001-06-13.
- Submission: K010986
- Applicant / Sponsor: Lunapads International Products, Ltd.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class I
- Regulation citation: 21 CFR 884.5435
- Decision date: 2001-06-13
Classification & Regulation
This clearance is catalogued under FDA product code NUQ and 21 CFR 884.5435, within the Obstetrics/Gynecology review panel as a Class I device.