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FDA 510(k)

FLOCHANNEL

K-Number: K081176 · 2008-07-28

ApplicantChad Therapeutics, Inc.
Decision Date2008-07-28
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FLOCHANNEL is the device name listed in this FDA 510(k) record. The listed applicant is Chad Therapeutics, Inc.. It received FDA 510(k) clearance on 2008-07-28 under 510(k) number K081176. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOCHANNEL?

FLOCHANNEL is a medical device that received FDA 510(k) clearance on 2008-07-28. The listed applicant is Chad Therapeutics, Inc.. The 510(k) number is K081176.

When did FLOCHANNEL receive FDA 510(k) clearance?

FLOCHANNEL received FDA 510(k) clearance on 2008-07-28, under 510(k) number K081176.

Who is the listed applicant for FLOCHANNEL?

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

What is the FDA product code for FLOCHANNEL?

The FDA product code for FLOCHANNEL is MNR.

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Other records listing Chad Therapeutics, Inc. as applicant

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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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