Clearance Summary
VAGINAL RETRACTOR received FDA 510(k) clearance under submission number K780349, sponsored by Edward Weck, Inc.. 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 1978-03-14.
- Submission: K780349
- Applicant / Sponsor: Edward Weck, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class I
- Regulation citation: 21 CFR 884.4520
- Decision date: 1978-03-14
Classification & Regulation
This clearance is catalogued under FDA product code HDL and 21 CFR 884.4520, within the Obstetrics/Gynecology review panel as a Class I device.