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FDA 510(k)

ACUSON L538 TRANSDUCER

K-Number: K883752 · 1988-12-01

ApplicantAcuson Corp.
Decision Date1988-12-01
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACUSON L538 TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Acuson Corp.. It received FDA 510(k) clearance on 1988-12-01 under 510(k) number K883752. 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 ACUSON L538 TRANSDUCER?

ACUSON L538 TRANSDUCER is a medical device that received FDA 510(k) clearance on 1988-12-01. The listed applicant is Acuson Corp.. The 510(k) number is K883752.

When did ACUSON L538 TRANSDUCER receive FDA 510(k) clearance?

ACUSON L538 TRANSDUCER received FDA 510(k) clearance on 1988-12-01, under 510(k) number K883752.

Who is the listed applicant for ACUSON L538 TRANSDUCER?

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

What is the FDA product code for ACUSON L538 TRANSDUCER?

The FDA product code for ACUSON L538 TRANSDUCER 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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