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FDA 510(k)

RX UNIVERSAL

K-Number: K822950 · 1982-10-22

ApplicantJeneric Ind.
Decision Date1982-10-22
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RX UNIVERSAL is the device name listed in this FDA 510(k) record. The listed applicant is Jeneric Ind.. It received FDA 510(k) clearance on 1982-10-22 under 510(k) number K822950. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RX UNIVERSAL?

RX UNIVERSAL is a medical device that received FDA 510(k) clearance on 1982-10-22. The listed applicant is Jeneric Ind.. The 510(k) number is K822950.

When did RX UNIVERSAL receive FDA 510(k) clearance?

RX UNIVERSAL received FDA 510(k) clearance on 1982-10-22, under 510(k) number K822950.

Who is the listed applicant for RX UNIVERSAL?

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 RX UNIVERSAL?

The FDA product code for RX UNIVERSAL is EJS.

Related Clinical Trials

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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.

K862822REXILLIUM N. B. F.K862926SURGICAL VITEXK854878H40 BASE METAL ALLOYK844122RX CBGK844123RX CBYK840561RX ELAN

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Related Devices (Code: EJS)

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.

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KGK022252STERNGOLD 1, MODEL 1127781SterngoldK022469ECO E4Wieland Dental + Technik GmbH & Co. KGK021367STERNGOLD 66, MODEL #1180230SterngoldK020195SIMIDUR S1SWieland Dental + Technik GmbH & Co. KG

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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