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FDA 510(k)

OMS QUARTZ INFUSION CONTACT LENS

K-Number: K820223 · 1982-02-05

ApplicantOptical Micro Systems, Inc.
Decision Date1982-02-05
Product CodeHJI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OMS QUARTZ INFUSION CONTACT LENS 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 1982-02-05 under 510(k) number K820223. The device is classified under product code HJI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMS QUARTZ INFUSION CONTACT LENS?

OMS QUARTZ INFUSION CONTACT LENS is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is Optical Micro Systems, Inc.. The 510(k) number is K820223.

When did OMS QUARTZ INFUSION CONTACT LENS receive FDA 510(k) clearance?

OMS QUARTZ INFUSION CONTACT LENS received FDA 510(k) clearance on 1982-02-05, under 510(k) number K820223.

Who is the listed applicant for OMS QUARTZ INFUSION CONTACT LENS?

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

What is the FDA product code for OMS QUARTZ INFUSION CONTACT LENS?

The FDA product code for OMS QUARTZ INFUSION CONTACT LENS is HJI.

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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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Related Devices (Code: HJI)

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.

K923670BYRNE EXPULSIVE LENSOcular Instruments, Inc.K902138STRIPE PROJECTORAcademic Catalyst Corp.K90183960 FUNDUS CAMERA CF-60UVCanon USA, Inc.K897186LASER IMAGING WORK STATIONInnovision Medical, Inc.K802927SEBESTYEN IRRIGATING CONTACT LENSCooper Medical Devices Corp.K802971LANDERS CONTACT LENSCooper Medical Devices Corp.

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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