K813483Substantially Equivalent

Oms Anterior Chamber Infusion Needle

Name: K813483 Oms Anterior Chamber Infusion Needle
Creator: Optical Micro Systems, Inc.
Published: 1982-01-22
License: https://open.fda.gov/license/

Optical Micro Systems, Inc., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K813483 is the FDA 510(k) clearance record for OMS ANTERIOR CHAMBER INFUSION NEEDLE, cleared for Optical Micro Systems, Inc. on 1982-01-22. FDA records list 21 510(k) clearances for Optical Micro Systems, Inc., from 1981-12-31 to 1995-07-17. As of 2026-09-10, FDA records show no recalls naming K813483.

Clearance record

Decision date: 1982-01-22
Received: 1981-12-01 (52 days to decision)
Review panel: Unknown
Applicant: Optical Micro Systems, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No