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FDA 510(k)

TRANSDUCERS, EUP-C318/V33/F334/CC331/B31/032T

K-Number: K910268 · 1991-04-15

ApplicantHitachi Medical Corp.
Decision Date1991-04-15
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TRANSDUCERS, EUP-C318/V33/F334/CC331/B31/032T is the device name listed in this FDA 510(k) record. The listed applicant is Hitachi Medical Corp.. It received FDA 510(k) clearance on 1991-04-15 under 510(k) number K910268. 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 TRANSDUCERS, EUP-C318/V33/F334/CC331/B31/032T?

TRANSDUCERS, EUP-C318/V33/F334/CC331/B31/032T is a medical device that received FDA 510(k) clearance on 1991-04-15. The listed applicant is Hitachi Medical Corp.. The 510(k) number is K910268.

When did TRANSDUCERS, EUP-C318/V33/F334/CC331/B31/032T receive FDA 510(k) clearance?

TRANSDUCERS, EUP-C318/V33/F334/CC331/B31/032T received FDA 510(k) clearance on 1991-04-15, under 510(k) number K910268.

Who is the listed applicant for TRANSDUCERS, EUP-C318/V33/F334/CC331/B31/032T?

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

What is the FDA product code for TRANSDUCERS, EUP-C318/V33/F334/CC331/B31/032T?

The FDA product code for TRANSDUCERS, EUP-C318/V33/F334/CC331/B31/032T is ITX.

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Other records listing Hitachi Medical 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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