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FDA 510(k)

METRIFLOW AFM-100 PERIPHERAL VASCULAR BLOOD FLOWME

K-Number: K853952 · 1987-01-05

ApplicantMetriflow, Inc.
Decision Date1987-01-05
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

METRIFLOW AFM-100 PERIPHERAL VASCULAR BLOOD FLOWME is the device name listed in this FDA 510(k) record. The listed applicant is Metriflow, Inc.. It received FDA 510(k) clearance on 1987-01-05 under 510(k) number K853952. 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 METRIFLOW AFM-100 PERIPHERAL VASCULAR BLOOD FLOWME?

METRIFLOW AFM-100 PERIPHERAL VASCULAR BLOOD FLOWME is a medical device that received FDA 510(k) clearance on 1987-01-05. The listed applicant is Metriflow, Inc.. The 510(k) number is K853952.

When did METRIFLOW AFM-100 PERIPHERAL VASCULAR BLOOD FLOWME receive FDA 510(k) clearance?

METRIFLOW AFM-100 PERIPHERAL VASCULAR BLOOD FLOWME received FDA 510(k) clearance on 1987-01-05, under 510(k) number K853952.

Who is the listed applicant for METRIFLOW AFM-100 PERIPHERAL VASCULAR BLOOD FLOWME?

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

What is the FDA product code for METRIFLOW AFM-100 PERIPHERAL VASCULAR BLOOD FLOWME?

The FDA product code for METRIFLOW AFM-100 PERIPHERAL VASCULAR BLOOD FLOWME is DPW.

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Related Devices (Code: DPW)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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