Clearance Summary
ASMOTOM AUTOMATED TREPHINE SYSTEM received FDA 510(k) clearance under submission number K013151, sponsored by Bkg Opthalmics USA, 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 2001-12-14.
- Submission: K013151
- Applicant / Sponsor: Bkg Opthalmics USA, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.4070
- Decision date: 2001-12-14
Classification & Regulation
This clearance is catalogued under FDA product code HRG and 21 CFR 886.4070, within the Ophthalmic review panel as a Class I device.