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FDA 510(k)

MEDTRONIC BIO-MEDICUS HANDCRANK MODEL 150

K-Number: K926357 · 1993-06-02

ApplicantMedtronic Bio-Medicus, Inc.
Decision Date1993-06-02
Product CodeDWA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC BIO-MEDICUS HANDCRANK MODEL 150 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 1993-06-02 under 510(k) number K926357. 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 HANDCRANK MODEL 150?

MEDTRONIC BIO-MEDICUS HANDCRANK MODEL 150 is a medical device that received FDA 510(k) clearance on 1993-06-02. The listed applicant is Medtronic Bio-Medicus, Inc.. The 510(k) number is K926357.

When did MEDTRONIC BIO-MEDICUS HANDCRANK MODEL 150 receive FDA 510(k) clearance?

MEDTRONIC BIO-MEDICUS HANDCRANK MODEL 150 received FDA 510(k) clearance on 1993-06-02, under 510(k) number K926357.

Who is the listed applicant for MEDTRONIC BIO-MEDICUS HANDCRANK MODEL 150?

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 HANDCRANK MODEL 150?

The FDA product code for MEDTRONIC BIO-MEDICUS HANDCRANK MODEL 150 is 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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