FDA 510(k)

OFTALMOGRAF

K-Number: K833024 · 1984-04-26

Decision Date1984-04-26

Product Code

DecisionSubstantially Equivalent

Device Summary

OFTALMOGRAF is the device name listed in this FDA 510(k) record. The listed applicant is Universal Instruments Corp.. It received FDA 510(k) clearance on 1984-04-26 under 510(k) number K833024. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OFTALMOGRAF?

OFTALMOGRAF is a medical device that received FDA 510(k) clearance on 1984-04-26. The listed applicant is Universal Instruments Corp.. The 510(k) number is K833024.

When did OFTALMOGRAF receive FDA 510(k) clearance?

OFTALMOGRAF received FDA 510(k) clearance on 1984-04-26, under 510(k) number K833024.

Who is the listed applicant for OFTALMOGRAF?

The FDA 510(k) record lists Universal Instruments Corp. 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 Universal Instruments Corp. as applicant

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Official Source

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