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FDA 510(k)

OLYMPUS LUS ULTRASONIC LITHOTRIPTER

K-Number: K873367 · 1987-11-30

ApplicantOlympus Corp.
Decision Date1987-11-30
Product CodeFEO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OLYMPUS LUS ULTRASONIC LITHOTRIPTER is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1987-11-30 under 510(k) number K873367. The device is classified under product code FEO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS LUS ULTRASONIC LITHOTRIPTER?

OLYMPUS LUS ULTRASONIC LITHOTRIPTER is a medical device that received FDA 510(k) clearance on 1987-11-30. The listed applicant is Olympus Corp.. The 510(k) number is K873367.

When did OLYMPUS LUS ULTRASONIC LITHOTRIPTER receive FDA 510(k) clearance?

OLYMPUS LUS ULTRASONIC LITHOTRIPTER received FDA 510(k) clearance on 1987-11-30, under 510(k) number K873367.

Who is the listed applicant for OLYMPUS LUS ULTRASONIC LITHOTRIPTER?

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 LUS ULTRASONIC LITHOTRIPTER?

The FDA product code for OLYMPUS LUS ULTRASONIC LITHOTRIPTER is FEO.

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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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