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FDA 510(k)

EZC MEDICAL, LLC INTUBAIDFLEX

K-Number: K090777 · 2009-08-04

ApplicantEzc Medical, LLC
Decision Date2009-08-04
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EZC MEDICAL, LLC INTUBAIDFLEX is the device name listed in this FDA 510(k) record. The listed applicant is Ezc Medical, LLC. It received FDA 510(k) clearance on 2009-08-04 under 510(k) number K090777. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZC MEDICAL, LLC INTUBAIDFLEX?

EZC MEDICAL, LLC INTUBAIDFLEX is a medical device that received FDA 510(k) clearance on 2009-08-04. The listed applicant is Ezc Medical, LLC. The 510(k) number is K090777.

When did EZC MEDICAL, LLC INTUBAIDFLEX receive FDA 510(k) clearance?

EZC MEDICAL, LLC INTUBAIDFLEX received FDA 510(k) clearance on 2009-08-04, under 510(k) number K090777.

Who is the listed applicant for EZC MEDICAL, LLC INTUBAIDFLEX?

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

What is the FDA product code for EZC MEDICAL, LLC INTUBAIDFLEX?

The FDA product code for EZC MEDICAL, LLC INTUBAIDFLEX is BTR.

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Official Source

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