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FDA 510(k)

MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540-D

K-Number: K914754 · 1992-05-20

ApplicantMedtronic Bio-Medicus, Inc.
Decision Date1992-05-20
Product CodeDWA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540-D is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Bio-Medicus, Inc.. It received FDA 510(k) clearance on 1992-05-20 under 510(k) number K914754. The device is classified under product code DWA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540-D?

MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540-D is a medical device that received FDA 510(k) clearance on 1992-05-20. The listed applicant is Medtronic Bio-Medicus, Inc.. The 510(k) number is K914754.

When did MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540-D receive FDA 510(k) clearance?

MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540-D received FDA 510(k) clearance on 1992-05-20, under 510(k) number K914754.

Who is the listed applicant for MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540-D?

The FDA 510(k) record lists Medtronic Bio-Medicus, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540-D?

The FDA product code for MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540-D is DWA.

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Other records listing Medtronic Bio-Medicus, Inc. as applicant

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Related Devices (Code: DWA)

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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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