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FDA 510(k)

L582 TRANSDUCER

K-Number: K904600 · 1991-06-24

ApplicantAcuson Corp.
Decision Date1991-06-24
Product CodeMAA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

L582 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 1991-06-24 under 510(k) number K904600. The device is classified under product code MAA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the L582 TRANSDUCER?

L582 TRANSDUCER is a medical device that received FDA 510(k) clearance on 1991-06-24. The listed applicant is Acuson Corp.. The 510(k) number is K904600.

When did L582 TRANSDUCER receive FDA 510(k) clearance?

L582 TRANSDUCER received FDA 510(k) clearance on 1991-06-24, under 510(k) number K904600.

Who is the listed applicant for L582 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 L582 TRANSDUCER?

The FDA product code for L582 TRANSDUCER is MAA.

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Other records listing Acuson Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K023772KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEMK022896CSV12 SOFTWARE VIEWERK022567SEQUOIA SIGNATURE II DIAGNOSTIC ULTRASOUND SYSTEMK021497CYPRESS ULTRASOUND SYSTEMK010950CYPRESS SYSTEMK0028073D ORGAN ASSESSMENT W/ MAGNETIC POSITION SENSING

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Related Devices (Code: MAA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K102138ULTRASONIC TABLETOP DOPPLER; ULTRASONIC TABLETOP DOPPLEREdan Instruments, Inc.K090499LIFEDOP MODEL, L350RSummit Doppler Systems, Inc.K915138GE SONOCHROMEGE Medical SystemsK905536FETAL DOPPLERToshiba America Medical Systems, In.CK905456L328 TRANSDUCERAcuson Corp.K904951S5192R TRANSDUCERAcuson Corp.

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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