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FDA 510(k)

MODEL IV6000 INFUSION PUMP

K-Number: K790332 · 1979-04-10

ApplicantValleylab, Inc.
Decision Date1979-04-10
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL IV6000 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 1979-04-10 under 510(k) number K790332. 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 MODEL IV6000 INFUSION PUMP?

MODEL IV6000 INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1979-04-10. The listed applicant is Valleylab, Inc.. The 510(k) number is K790332.

When did MODEL IV6000 INFUSION PUMP receive FDA 510(k) clearance?

MODEL IV6000 INFUSION PUMP received FDA 510(k) clearance on 1979-04-10, under 510(k) number K790332.

Who is the listed applicant for MODEL IV6000 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 MODEL IV6000 INFUSION PUMP?

The FDA product code for MODEL IV6000 INFUSION PUMP is 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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