FDA 510(k)

INTRAOCULAR LENS

K-Number: K770728 · 1977-04-28

Decision Date1977-04-28

Product Code

DecisionSubstantially Equivalent

Device Summary

INTRAOCULAR LENS is the device name listed in this FDA 510(k) record. The listed applicant is Milton Roy Co. Analytical. It received FDA 510(k) clearance on 1977-04-28 under 510(k) number K770728. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRAOCULAR LENS?

INTRAOCULAR LENS is a medical device that received FDA 510(k) clearance on 1977-04-28. The listed applicant is Milton Roy Co. Analytical. The 510(k) number is K770728.

When did INTRAOCULAR LENS receive FDA 510(k) clearance?

INTRAOCULAR LENS received FDA 510(k) clearance on 1977-04-28, under 510(k) number K770728.

Who is the listed applicant for INTRAOCULAR LENS?

The FDA 510(k) record lists Milton Roy Co. Analytical 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 Milton Roy Co. Analytical as applicant

K771065DYLADE, MODEL DS

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.