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FDA 510(k)

INTAVENT LARYNGEAL MASK

K-Number: K904834 · 1991-07-26

ApplicantIntavent Intl. S.A.
Decision Date1991-07-26
Product CodeCAE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INTAVENT LARYNGEAL MASK is the device name listed in this FDA 510(k) record. The listed applicant is Intavent Intl. S.A.. It received FDA 510(k) clearance on 1991-07-26 under 510(k) number K904834. The device is classified under product code CAE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTAVENT LARYNGEAL MASK?

INTAVENT LARYNGEAL MASK is a medical device that received FDA 510(k) clearance on 1991-07-26. The listed applicant is Intavent Intl. S.A.. The 510(k) number is K904834.

When did INTAVENT LARYNGEAL MASK receive FDA 510(k) clearance?

INTAVENT LARYNGEAL MASK received FDA 510(k) clearance on 1991-07-26, under 510(k) number K904834.

Who is the listed applicant for INTAVENT LARYNGEAL MASK?

The FDA 510(k) record lists Intavent Intl. S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTAVENT LARYNGEAL MASK?

The FDA product code for INTAVENT LARYNGEAL MASK is CAE.

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Related Devices (Code: CAE)

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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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