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FDA 510(k)

OCULAR OCCLUDER

K-Number: K900942 · 1990-05-25

ApplicantMicrodynamics
Decision Date1990-05-25
Product CodeHOY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OCULAR OCCLUDER is the device name listed in this FDA 510(k) record. The listed applicant is Microdynamics. It received FDA 510(k) clearance on 1990-05-25 under 510(k) number K900942. The device is classified under product code HOY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OCULAR OCCLUDER?

OCULAR OCCLUDER is a medical device that received FDA 510(k) clearance on 1990-05-25. The listed applicant is Microdynamics. The 510(k) number is K900942.

When did OCULAR OCCLUDER receive FDA 510(k) clearance?

OCULAR OCCLUDER received FDA 510(k) clearance on 1990-05-25, under 510(k) number K900942.

Who is the listed applicant for OCULAR OCCLUDER?

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

What is the FDA product code for OCULAR OCCLUDER?

The FDA product code for OCULAR OCCLUDER is HOY.

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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.

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