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FDA 510(k)

CERAL-BASE METAL ALLOY

K-Number: K813243 · 1981-12-31

ApplicantSillard Products, Inc.
Decision Date1981-12-31
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERAL-BASE METAL ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Sillard Products, Inc.. It received FDA 510(k) clearance on 1981-12-31 under 510(k) number K813243. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERAL-BASE METAL ALLOY?

CERAL-BASE METAL ALLOY is a medical device that received FDA 510(k) clearance on 1981-12-31. The listed applicant is Sillard Products, Inc.. The 510(k) number is K813243.

When did CERAL-BASE METAL ALLOY receive FDA 510(k) clearance?

CERAL-BASE METAL ALLOY received FDA 510(k) clearance on 1981-12-31, under 510(k) number K813243.

Who is the listed applicant for CERAL-BASE METAL ALLOY?

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

What is the FDA product code for CERAL-BASE METAL ALLOY?

The FDA product code for CERAL-BASE METAL ALLOY is EJH.

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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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