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FDA 510(k)

A16 BLOOD FLOW MEASUREMENT SYSTEM

K-Number: K023707 · 2003-02-12

ApplicantD. E. Hokanson, Inc.
Decision Date2003-02-12
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

A16 BLOOD FLOW MEASUREMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is D. E. Hokanson, Inc.. It received FDA 510(k) clearance on 2003-02-12 under 510(k) number K023707. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A16 BLOOD FLOW MEASUREMENT SYSTEM?

A16 BLOOD FLOW MEASUREMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2003-02-12. The listed applicant is D. E. Hokanson, Inc.. The 510(k) number is K023707.

When did A16 BLOOD FLOW MEASUREMENT SYSTEM receive FDA 510(k) clearance?

A16 BLOOD FLOW MEASUREMENT SYSTEM received FDA 510(k) clearance on 2003-02-12, under 510(k) number K023707.

Who is the listed applicant for A16 BLOOD FLOW MEASUREMENT SYSTEM?

The FDA 510(k) record lists D. E. Hokanson, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A16 BLOOD FLOW MEASUREMENT SYSTEM?

The FDA product code for A16 BLOOD FLOW MEASUREMENT SYSTEM is JOM.

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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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