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FDA 510(k)

IV7200 AND IV7400 INFUSION PUMP

K-Number: K860694 · 1986-04-22

ApplicantValleylab, Inc.
Decision Date1986-04-22
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV7200 AND IV7400 INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1986-04-22 under 510(k) number K860694. 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 IV7200 AND IV7400 INFUSION PUMP?

IV7200 AND IV7400 INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1986-04-22. The listed applicant is Valleylab, Inc.. The 510(k) number is K860694.

When did IV7200 AND IV7400 INFUSION PUMP receive FDA 510(k) clearance?

IV7200 AND IV7400 INFUSION PUMP received FDA 510(k) clearance on 1986-04-22, under 510(k) number K860694.

Who is the listed applicant for IV7200 AND IV7400 INFUSION PUMP?

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

What is the FDA product code for IV7200 AND IV7400 INFUSION PUMP?

The FDA product code for IV7200 AND IV7400 INFUSION PUMP is FRN.

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Related Devices (Code: FRN)

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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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