FDA 510(k)

RX CBG

K-Number: K844122 · 1985-01-09

Decision Date1985-01-09

Product CodeEJH

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

RX CBG is the device name listed in this FDA 510(k) record. The listed applicant is Jeneric Ind.. It received FDA 510(k) clearance on 1985-01-09 under 510(k) number K844122. 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 RX CBG?

RX CBG is a medical device that received FDA 510(k) clearance on 1985-01-09. The listed applicant is Jeneric Ind.. The 510(k) number is K844122.

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

RX CBG received FDA 510(k) clearance on 1985-01-09, under 510(k) number K844122.

Who is the listed applicant for RX CBG?

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 CBG?

The FDA product code for RX CBG is EJH.

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 K844123RX CBY K840561RX ELAN K840563RX C & B 20

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Official Source

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