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FDA 510(k)

BELSCOPE LARYNGOSCOPE

K-Number: K904918 · 1991-07-22

ApplicantAvulunga Pty. , Ltd.
Decision Date1991-07-22
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BELSCOPE LARYNGOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Avulunga Pty. , Ltd.. It received FDA 510(k) clearance on 1991-07-22 under 510(k) number K904918. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BELSCOPE LARYNGOSCOPE?

BELSCOPE LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1991-07-22. The listed applicant is Avulunga Pty. , Ltd.. The 510(k) number is K904918.

When did BELSCOPE LARYNGOSCOPE receive FDA 510(k) clearance?

BELSCOPE LARYNGOSCOPE received FDA 510(k) clearance on 1991-07-22, under 510(k) number K904918.

Who is the listed applicant for BELSCOPE LARYNGOSCOPE?

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

What is the FDA product code for BELSCOPE LARYNGOSCOPE?

The FDA product code for BELSCOPE LARYNGOSCOPE is CCW.

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Related Devices (Code: CCW)

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

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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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