FDA 510(k)

AO FLEXIBLE LARYNGOSCOPE, #LS-7

K-Number: K802331 · 1980-10-10

Decision Date1980-10-10

Product CodeCAL

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

AO FLEXIBLE LARYNGOSCOPE, #LS-7 is the device name listed in this FDA 510(k) record. The listed applicant is American Optical Corp.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802331. The device is classified under product code CAL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AO FLEXIBLE LARYNGOSCOPE, #LS-7?

AO FLEXIBLE LARYNGOSCOPE, #LS-7 is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is American Optical Corp.. The 510(k) number is K802331.

When did AO FLEXIBLE LARYNGOSCOPE, #LS-7 receive FDA 510(k) clearance?

AO FLEXIBLE LARYNGOSCOPE, #LS-7 received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802331.

Who is the listed applicant for AO FLEXIBLE LARYNGOSCOPE, #LS-7?

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

What is the FDA product code for AO FLEXIBLE LARYNGOSCOPE, #LS-7?

The FDA product code for AO FLEXIBLE LARYNGOSCOPE, #LS-7 is CAL.

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Other records listing American Optical Corp. as applicant

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Related Devices (Code: CAL)

K951194FI-10MPentax Precision Instrument Corp.K951195FI-10PPentax Precision Instrument Corp.K872895HAEMONETICS CELL SAVER MINI SAVER AUTO. BLOOD SYS.Haemonetics Corp.K852994REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11Reichert-Jung, Inc.K850978OLYMPUS LF-1 INTUBATION SCOPEOlympus Corp.K801364AO STYLET LARYNGOSCOPE MODEL SLSAmerican Optical Corp.

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.