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FDA 510(k)

OMS ANTERIOR CHAMBER INFUSION NEEDLE

K-Number: K813483 · 1982-01-22

ApplicantOptical Micro Systems, Inc.
Decision Date1982-01-22
Product Code
DecisionSubstantially Equivalent

Device Summary

OMS ANTERIOR CHAMBER INFUSION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Optical Micro Systems, Inc.. It received FDA 510(k) clearance on 1982-01-22 under 510(k) number K813483. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMS ANTERIOR CHAMBER INFUSION NEEDLE?

OMS ANTERIOR CHAMBER INFUSION NEEDLE is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Optical Micro Systems, Inc.. The 510(k) number is K813483.

When did OMS ANTERIOR CHAMBER INFUSION NEEDLE receive FDA 510(k) clearance?

OMS ANTERIOR CHAMBER INFUSION NEEDLE received FDA 510(k) clearance on 1982-01-22, under 510(k) number K813483.

Who is the listed applicant for OMS ANTERIOR CHAMBER INFUSION NEEDLE?

The FDA 510(k) record lists Optical Micro Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Optical Micro Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K950218OMS SLIMLINE PHACO HANDPIECEK946054DIPLOMAXK935223OPHTHALMIC SURGICAL SYSTEMK935226I/V POLEK935003ELECTRIC I/V POLE OR EIVP2K870068ASPIRATION REVERSAL CONTROL (ARC) MODULE

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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