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FDA 510(k)

FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber

K-Number: K240569 · 2024-11-21

ApplicantFink Engineering Pty, Ltd.
Decision Date2024-11-21
Product CodeCBF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber is the device name listed in this FDA 510(k) record. The listed applicant is Fink Engineering Pty, Ltd.. It received FDA 510(k) clearance on 2024-11-21 under 510(k) number K240569. 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 FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber?

FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber is a medical device that received FDA 510(k) clearance on 2024-11-21. The listed applicant is Fink Engineering Pty, Ltd.. The 510(k) number is K240569.

When did FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber receive FDA 510(k) clearance?

FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber received FDA 510(k) clearance on 2024-11-21, under 510(k) number K240569.

Who is the listed applicant for FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber?

The FDA 510(k) record lists Fink Engineering Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber?

The FDA product code for FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber is CBF.

Related Devices (Code: CBF)

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.

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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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