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FDA 510(k)

NKA MODEL MFV-3100 & MFV-3200 ELECTRO. BLOOD FLOW.

K-Number: K894631 · 1990-01-19

ApplicantNihon Kohden America, Inc.
Decision Date1990-01-19
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NKA MODEL MFV-3100 & MFV-3200 ELECTRO. BLOOD FLOW. is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden America, Inc.. It received FDA 510(k) clearance on 1990-01-19 under 510(k) number K894631. 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 NKA MODEL MFV-3100 & MFV-3200 ELECTRO. BLOOD FLOW.?

NKA MODEL MFV-3100 & MFV-3200 ELECTRO. BLOOD FLOW. is a medical device that received FDA 510(k) clearance on 1990-01-19. The listed applicant is Nihon Kohden America, Inc.. The 510(k) number is K894631.

When did NKA MODEL MFV-3100 & MFV-3200 ELECTRO. BLOOD FLOW. receive FDA 510(k) clearance?

NKA MODEL MFV-3100 & MFV-3200 ELECTRO. BLOOD FLOW. received FDA 510(k) clearance on 1990-01-19, under 510(k) number K894631.

Who is the listed applicant for NKA MODEL MFV-3100 & MFV-3200 ELECTRO. BLOOD FLOW.?

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

What is the FDA product code for NKA MODEL MFV-3100 & MFV-3200 ELECTRO. BLOOD FLOW.?

The FDA product code for NKA MODEL MFV-3100 & MFV-3200 ELECTRO. BLOOD FLOW. is DPW.

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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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