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FDA 510(k)

REXILLIUM III

K-Number: K833143 · 1983-12-08

ApplicantJeneric Ind.
Decision Date1983-12-08
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

REXILLIUM III is the device name listed in this FDA 510(k) record. The listed applicant is Jeneric Ind.. It received FDA 510(k) clearance on 1983-12-08 under 510(k) number K833143. 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 REXILLIUM III?

REXILLIUM III is a medical device that received FDA 510(k) clearance on 1983-12-08. The listed applicant is Jeneric Ind.. The 510(k) number is K833143.

When did REXILLIUM III receive FDA 510(k) clearance?

REXILLIUM III received FDA 510(k) clearance on 1983-12-08, under 510(k) number K833143.

Who is the listed applicant for REXILLIUM III?

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 REXILLIUM III?

The FDA product code for REXILLIUM III 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.

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

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Related Devices (Code: EJH)

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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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