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FDA 510(k)

L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC

K-Number: K904901 · 1991-03-26

ApplicantParexel Intl. Corp.
Decision Date1991-03-26
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC is the device name listed in this FDA 510(k) record. The listed applicant is Parexel Intl. Corp.. It received FDA 510(k) clearance on 1991-03-26 under 510(k) number K904901. 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 L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC?

L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC is a medical device that received FDA 510(k) clearance on 1991-03-26. The listed applicant is Parexel Intl. Corp.. The 510(k) number is K904901.

When did L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC receive FDA 510(k) clearance?

L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC received FDA 510(k) clearance on 1991-03-26, under 510(k) number K904901.

Who is the listed applicant for L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC?

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

What is the FDA product code for L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC?

The FDA product code for L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC is ITX.

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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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