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FDA 510(k)

RARE-EARTH INTRA-OCULAR MAGNET

K-Number: K831702 · 1983-06-30

Decision Date1983-06-30
Product CodeHPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RARE-EARTH INTRA-OCULAR MAGNET is the device name listed in this FDA 510(k) record. The listed applicant is Miami Eye Technology, Inc.. It received FDA 510(k) clearance on 1983-06-30 under 510(k) number K831702. The device is classified under product code HPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RARE-EARTH INTRA-OCULAR MAGNET?

RARE-EARTH INTRA-OCULAR MAGNET is a medical device that received FDA 510(k) clearance on 1983-06-30. The listed applicant is Miami Eye Technology, Inc.. The 510(k) number is K831702.

When did RARE-EARTH INTRA-OCULAR MAGNET receive FDA 510(k) clearance?

RARE-EARTH INTRA-OCULAR MAGNET received FDA 510(k) clearance on 1983-06-30, under 510(k) number K831702.

Who is the listed applicant for RARE-EARTH INTRA-OCULAR MAGNET?

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

What is the FDA product code for RARE-EARTH INTRA-OCULAR MAGNET?

The FDA product code for RARE-EARTH INTRA-OCULAR MAGNET is HPN.

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.

Other records listing Miami Eye Technology, 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.

Related Devices (Code: HPN)

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.

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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