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FDA 510(k)

INTEGRITY EYE DROP GUIDE

K-Number: K851908 · 1985-06-03

ApplicantIntegrity Optics, Inc.
Decision Date1985-06-03
Product Code
DecisionSubstantially Equivalent

Device Summary

INTEGRITY EYE DROP GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Integrity Optics, Inc.. It received FDA 510(k) clearance on 1985-06-03 under 510(k) number K851908. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTEGRITY EYE DROP GUIDE?

INTEGRITY EYE DROP GUIDE is a medical device that received FDA 510(k) clearance on 1985-06-03. The listed applicant is Integrity Optics, Inc.. The 510(k) number is K851908.

When did INTEGRITY EYE DROP GUIDE receive FDA 510(k) clearance?

INTEGRITY EYE DROP GUIDE received FDA 510(k) clearance on 1985-06-03, under 510(k) number K851908.

Who is the listed applicant for INTEGRITY EYE DROP GUIDE?

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

Related Clinical Trials

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.

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Other records listing Integrity Optics, 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.

K853199INTEGRITY EYE DROP GUIDE(MODIFICATION)

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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