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FDA 510(k)

OLYMPUS EU-M30 ENDOSCOPIC ULTRASOUND CENTER

K-Number: K951994 · 1996-04-15

ApplicantOlympus America, Inc.
Decision Date1996-04-15
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

OLYMPUS EU-M30 ENDOSCOPIC ULTRASOUND CENTER is the device name listed in this FDA 510(k) record. The listed applicant is Olympus America, Inc.. It received FDA 510(k) clearance on 1996-04-15 under 510(k) number K951994. 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 EU-M30 ENDOSCOPIC ULTRASOUND CENTER?

OLYMPUS EU-M30 ENDOSCOPIC ULTRASOUND CENTER is a medical device that received FDA 510(k) clearance on 1996-04-15. The listed applicant is Olympus America, Inc.. The 510(k) number is K951994.

When did OLYMPUS EU-M30 ENDOSCOPIC ULTRASOUND CENTER receive FDA 510(k) clearance?

OLYMPUS EU-M30 ENDOSCOPIC ULTRASOUND CENTER received FDA 510(k) clearance on 1996-04-15, under 510(k) number K951994.

Who is the listed applicant for OLYMPUS EU-M30 ENDOSCOPIC ULTRASOUND CENTER?

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

What is the FDA product code for OLYMPUS EU-M30 ENDOSCOPIC ULTRASOUND CENTER?

The FDA product code for OLYMPUS EU-M30 ENDOSCOPIC ULTRASOUND CENTER 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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