FDA 510(k)

RX C & B 20

K-Number: K840563 · 1984-05-01

Decision Date1984-05-01

Product CodeEJS

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

RX C & B 20 is the device name listed in this FDA 510(k) record. The listed applicant is Jeneric Ind.. It received FDA 510(k) clearance on 1984-05-01 under 510(k) number K840563. 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 C & B 20?

RX C & B 20 is a medical device that received FDA 510(k) clearance on 1984-05-01. The listed applicant is Jeneric Ind.. The 510(k) number is K840563.

When did RX C & B 20 receive FDA 510(k) clearance?

RX C & B 20 received FDA 510(k) clearance on 1984-05-01, under 510(k) number K840563.

Who is the listed applicant for RX C & B 20?

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 C & B 20?

The FDA product code for RX C & B 20 is EJS.

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 VITEX K854878H40 BASE METAL ALLOY K844122RX CBG K844123RX CBY K840561RX ELAN

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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.