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 a medical device manufactured by Fink Engineering Pty, Ltd.. It received FDA 510(k) clearance on 2024-11-21 under approval 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. It is manufactured by Fink Engineering Pty, Ltd.. The 510(k) number is K240569.
When was FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber approved by the FDA?
FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber received FDA 510(k) clearance on 2024-11-21, under approval number K240569.
What company makes FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber?
FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber is manufactured by Fink Engineering Pty, Ltd..
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)
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.