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FDA 510(k)

H40 BASE METAL ALLOY

K-Number: K854878 · 1986-01-30

ApplicantJeneric Ind.
Decision Date1986-01-30
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

H40 BASE METAL ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Jeneric Ind.. It received FDA 510(k) clearance on 1986-01-30 under 510(k) number K854878. 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 H40 BASE METAL ALLOY?

H40 BASE METAL ALLOY is a medical device that received FDA 510(k) clearance on 1986-01-30. The listed applicant is Jeneric Ind.. The 510(k) number is K854878.

When did H40 BASE METAL ALLOY receive FDA 510(k) clearance?

H40 BASE METAL ALLOY received FDA 510(k) clearance on 1986-01-30, under 510(k) number K854878.

Who is the listed applicant for H40 BASE METAL ALLOY?

The FDA 510(k) record lists Jeneric Ind. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for H40 BASE METAL ALLOY?

The FDA product code for H40 BASE METAL ALLOY is EJH.

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Other records listing Jeneric Ind. 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: EJH)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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