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FDA 510(k)

RENEAU UNIT

K-Number: K840841 · 1984-08-07

ApplicantReneau, Inc.
Decision Date1984-08-07
Product CodeCBF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RENEAU UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Reneau, Inc.. It received FDA 510(k) clearance on 1984-08-07 under 510(k) number K840841. The device is classified under product code CBF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RENEAU UNIT?

RENEAU UNIT is a medical device that received FDA 510(k) clearance on 1984-08-07. The listed applicant is Reneau, Inc.. The 510(k) number is K840841.

When did RENEAU UNIT receive FDA 510(k) clearance?

RENEAU UNIT received FDA 510(k) clearance on 1984-08-07, under 510(k) number K840841.

Who is the listed applicant for RENEAU UNIT?

The FDA 510(k) record lists Reneau, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RENEAU UNIT?

The FDA product code for RENEAU UNIT is CBF.

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Related Devices (Code: CBF)

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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.

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