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FDA 510(k)

ALLOY COMPOSITE POLISH

K-Number: K810912 · 1981-04-23

ApplicantMoyco Industries, Inc.
Decision Date1981-04-23
Product CodeEJR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ALLOY COMPOSITE POLISH is the device name listed in this FDA 510(k) record. The listed applicant is Moyco Industries, Inc.. It received FDA 510(k) clearance on 1981-04-23 under 510(k) number K810912. The device is classified under product code EJR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLOY COMPOSITE POLISH?

ALLOY COMPOSITE POLISH is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is Moyco Industries, Inc.. The 510(k) number is K810912.

When did ALLOY COMPOSITE POLISH receive FDA 510(k) clearance?

ALLOY COMPOSITE POLISH received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810912.

Who is the listed applicant for ALLOY COMPOSITE POLISH?

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

What is the FDA product code for ALLOY COMPOSITE POLISH?

The FDA product code for ALLOY COMPOSITE POLISH is EJR.

Related Clinical Trials

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Other records listing Moyco Industries, 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.

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Related Devices (Code: EJR)

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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