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FDA 510(k)

OLYMPUS JF-UM3-7.5/-12 AND CF-UM3-7.5/-12

K-Number: K900880 · 1991-04-29

ApplicantOlympus Corp.
Decision Date1991-04-29
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

OLYMPUS JF-UM3-7.5/-12 AND CF-UM3-7.5/-12 is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1991-04-29 under 510(k) number K900880. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS JF-UM3-7.5/-12 AND CF-UM3-7.5/-12?

OLYMPUS JF-UM3-7.5/-12 AND CF-UM3-7.5/-12 is a medical device that received FDA 510(k) clearance on 1991-04-29. The listed applicant is Olympus Corp.. The 510(k) number is K900880.

When did OLYMPUS JF-UM3-7.5/-12 AND CF-UM3-7.5/-12 receive FDA 510(k) clearance?

OLYMPUS JF-UM3-7.5/-12 AND CF-UM3-7.5/-12 received FDA 510(k) clearance on 1991-04-29, under 510(k) number K900880.

Who is the listed applicant for OLYMPUS JF-UM3-7.5/-12 AND CF-UM3-7.5/-12?

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 JF-UM3-7.5/-12 AND CF-UM3-7.5/-12?

The FDA product code for OLYMPUS JF-UM3-7.5/-12 AND CF-UM3-7.5/-12 is ITX.

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Other records listing Olympus Corp. as applicant

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Related Devices (Code: ITX)

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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.

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