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FDA 510(k)

DYLADE, MODEL DS

K-Number: K771065 · 1977-06-24

ApplicantMilton Roy Co. Analytical
Decision Date1977-06-24
Product CodeFKP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DYLADE, MODEL DS 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 1977-06-24 under 510(k) number K771065. The device is classified under product code FKP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYLADE, MODEL DS?

DYLADE, MODEL DS is a medical device that received FDA 510(k) clearance on 1977-06-24. The listed applicant is Milton Roy Co. Analytical. The 510(k) number is K771065.

When did DYLADE, MODEL DS receive FDA 510(k) clearance?

DYLADE, MODEL DS received FDA 510(k) clearance on 1977-06-24, under 510(k) number K771065.

Who is the listed applicant for DYLADE, MODEL DS?

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

What is the FDA product code for DYLADE, MODEL DS?

The FDA product code for DYLADE, MODEL DS is FKP.

Related Clinical Trials

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Other records listing Milton Roy Co. Analytical 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.

K770728INTRAOCULAR LENS

Related Devices (Code: FKP)

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

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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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