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FDA 510(k)

OCULOPRESSOR

K-Number: K832477 · 1983-08-16

ApplicantHans Gevder
Decision Date1983-08-16
Product Code
DecisionSubstantially Equivalent

Device Summary

OCULOPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Hans Gevder. It received FDA 510(k) clearance on 1983-08-16 under 510(k) number K832477. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OCULOPRESSOR?

OCULOPRESSOR is a medical device that received FDA 510(k) clearance on 1983-08-16. The listed applicant is Hans Gevder. The 510(k) number is K832477.

When did OCULOPRESSOR receive FDA 510(k) clearance?

OCULOPRESSOR received FDA 510(k) clearance on 1983-08-16, under 510(k) number K832477.

Who is the listed applicant for OCULOPRESSOR?

The FDA 510(k) record lists Hans Gevder 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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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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