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FDA 510(k)

OLYMPUS GF-UM2/EU-M2

K-Number: K872027 · 1987-08-17

ApplicantOlympus Corp.
Decision Date1987-08-17
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

OLYMPUS GF-UM2/EU-M2 is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1987-08-17 under 510(k) number K872027. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS GF-UM2/EU-M2?

OLYMPUS GF-UM2/EU-M2 is a medical device that received FDA 510(k) clearance on 1987-08-17. The listed applicant is Olympus Corp.. The 510(k) number is K872027.

When did OLYMPUS GF-UM2/EU-M2 receive FDA 510(k) clearance?

OLYMPUS GF-UM2/EU-M2 received FDA 510(k) clearance on 1987-08-17, under 510(k) number K872027.

Who is the listed applicant for OLYMPUS GF-UM2/EU-M2?

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 GF-UM2/EU-M2?

The FDA product code for OLYMPUS GF-UM2/EU-M2 is IYO.

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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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