Clearance Summary
61-100 TO 61-124 VARIOUS VAGINAL SPECVIA(CUSCO,GRA received FDA 510(k) clearance under submission number K851799, sponsored by Artiberia. 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 1985-05-22.
- Submission: K851799
- Applicant / Sponsor: Artiberia
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class I
- Regulation citation: 21 CFR 884.4520
- Decision date: 1985-05-22
Classification & Regulation
This clearance is catalogued under FDA product code HDF and 21 CFR 884.4520, within the Obstetrics/Gynecology review panel as a Class I device.