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FDA 510(k)

DVM-4200 BLOOD FLOWMETER

K-Number: K892707 · 1989-07-28

ApplicantKoven and Assoc., Inc.
Decision Date1989-07-28
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DVM-4200 BLOOD FLOWMETER is the device name listed in this FDA 510(k) record. The listed applicant is Koven and Assoc., Inc.. It received FDA 510(k) clearance on 1989-07-28 under 510(k) number K892707. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DVM-4200 BLOOD FLOWMETER?

DVM-4200 BLOOD FLOWMETER is a medical device that received FDA 510(k) clearance on 1989-07-28. The listed applicant is Koven and Assoc., Inc.. The 510(k) number is K892707.

When did DVM-4200 BLOOD FLOWMETER receive FDA 510(k) clearance?

DVM-4200 BLOOD FLOWMETER received FDA 510(k) clearance on 1989-07-28, under 510(k) number K892707.

Who is the listed applicant for DVM-4200 BLOOD FLOWMETER?

The FDA 510(k) record lists Koven and Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DVM-4200 BLOOD FLOWMETER?

The FDA product code for DVM-4200 BLOOD FLOWMETER is DPW.

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Other records listing Koven and Assoc., Inc. as applicant

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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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