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FDA 510(k)

VI-FLOW PUMP WITH VI-SET

K-Number: K851821 · 1985-07-05

ApplicantVital Canada, Inc.
Decision Date1985-07-05
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VI-FLOW PUMP WITH VI-SET is the device name listed in this FDA 510(k) record. The listed applicant is Vital Canada, Inc.. It received FDA 510(k) clearance on 1985-07-05 under 510(k) number K851821. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VI-FLOW PUMP WITH VI-SET?

VI-FLOW PUMP WITH VI-SET is a medical device that received FDA 510(k) clearance on 1985-07-05. The listed applicant is Vital Canada, Inc.. The 510(k) number is K851821.

When did VI-FLOW PUMP WITH VI-SET receive FDA 510(k) clearance?

VI-FLOW PUMP WITH VI-SET received FDA 510(k) clearance on 1985-07-05, under 510(k) number K851821.

Who is the listed applicant for VI-FLOW PUMP WITH VI-SET?

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

What is the FDA product code for VI-FLOW PUMP WITH VI-SET?

The FDA product code for VI-FLOW PUMP WITH VI-SET is FRN.

Related Devices (Code: FRN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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