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FDA 510(k)

REX ALLOY

K-Number: K833144 · 1983-10-28

ApplicantJeneric Ind.
Decision Date1983-10-28
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

REX 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 1983-10-28 under 510(k) number K833144. 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 REX ALLOY?

REX ALLOY is a medical device that received FDA 510(k) clearance on 1983-10-28. The listed applicant is Jeneric Ind.. The 510(k) number is K833144.

When did REX ALLOY receive FDA 510(k) clearance?

REX ALLOY received FDA 510(k) clearance on 1983-10-28, under 510(k) number K833144.

Who is the listed applicant for REX 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 REX ALLOY?

The FDA product code for REX 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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