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FDA 510(k)

THE FREMSTAD RING

K-Number: K982599 · 1999-02-16

ApplicantOphthalmic Solutions, LLC
Decision Date1999-02-16
Product CodeHOZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THE FREMSTAD RING is the device name listed in this FDA 510(k) record. The listed applicant is Ophthalmic Solutions, LLC. It received FDA 510(k) clearance on 1999-02-16 under 510(k) number K982599. The device is classified under product code HOZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE FREMSTAD RING?

THE FREMSTAD RING is a medical device that received FDA 510(k) clearance on 1999-02-16. The listed applicant is Ophthalmic Solutions, LLC. The 510(k) number is K982599.

When did THE FREMSTAD RING receive FDA 510(k) clearance?

THE FREMSTAD RING received FDA 510(k) clearance on 1999-02-16, under 510(k) number K982599.

Who is the listed applicant for THE FREMSTAD RING?

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

What is the FDA product code for THE FREMSTAD RING?

The FDA product code for THE FREMSTAD RING is HOZ.

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Related Devices (Code: HOZ)

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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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