Clearance Summary
POST-MYDS(TM) received FDA 510(k) clearance under submission number K930840, sponsored by Aukland Medical Plastics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1994-03-01.
- Submission: K930840
- Applicant / Sponsor: Aukland Medical Plastics, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.4750
- Decision date: 1994-03-01
Classification & Regulation
This clearance is catalogued under FDA product code HOY and 21 CFR 886.4750, within the Ophthalmic review panel as a Class I device.