FDA 510(k)

OLYMPUS LF-1 INTUBATION SCOPE

K-Number: K850978 · 1985-05-23

Decision Date1985-05-23

Product CodeCAL

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

OLYMPUS LF-1 INTUBATION SCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1985-05-23 under 510(k) number K850978. 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 OLYMPUS LF-1 INTUBATION SCOPE?

OLYMPUS LF-1 INTUBATION SCOPE is a medical device that received FDA 510(k) clearance on 1985-05-23. The listed applicant is Olympus Corp.. The 510(k) number is K850978.

When did OLYMPUS LF-1 INTUBATION SCOPE receive FDA 510(k) clearance?

OLYMPUS LF-1 INTUBATION SCOPE received FDA 510(k) clearance on 1985-05-23, under 510(k) number K850978.

Who is the listed applicant for OLYMPUS LF-1 INTUBATION SCOPE?

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

What is the FDA product code for OLYMPUS LF-1 INTUBATION SCOPE?

The FDA product code for OLYMPUS LF-1 INTUBATION SCOPE is CAL.

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Other records listing Olympus 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.K802331AO FLEXIBLE LARYNGOSCOPE, #LS-7American Optical 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.