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FDA 510(k)

LFRE INDIRECT LARYNGOSCOPE

K-Number: K023004 · 2003-01-28

ApplicantAstralite Corp.
Decision Date2003-01-28
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

LFRE INDIRECT LARYNGOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Astralite Corp.. It received FDA 510(k) clearance on 2003-01-28 under 510(k) number K023004. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LFRE INDIRECT LARYNGOSCOPE?

LFRE INDIRECT LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 2003-01-28. The listed applicant is Astralite Corp.. The 510(k) number is K023004.

When did LFRE INDIRECT LARYNGOSCOPE receive FDA 510(k) clearance?

LFRE INDIRECT LARYNGOSCOPE received FDA 510(k) clearance on 2003-01-28, under 510(k) number K023004.

Who is the listed applicant for LFRE INDIRECT LARYNGOSCOPE?

The FDA 510(k) record lists Astralite Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LFRE INDIRECT LARYNGOSCOPE?

The FDA product code for LFRE INDIRECT LARYNGOSCOPE is EOB.

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Other records listing Astralite Corp. as applicant

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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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