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FDA 510(k)

INFUTROL 7000 INFUSION PUMP

K-Number: K832008 · 1983-08-12

ApplicantValleylab, Inc.
Decision Date1983-08-12
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFUTROL 7000 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 1983-08-12 under 510(k) number K832008. 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 INFUTROL 7000 INFUSION PUMP?

INFUTROL 7000 INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Valleylab, Inc.. The 510(k) number is K832008.

When did INFUTROL 7000 INFUSION PUMP receive FDA 510(k) clearance?

INFUTROL 7000 INFUSION PUMP received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832008.

Who is the listed applicant for INFUTROL 7000 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 INFUTROL 7000 INFUSION PUMP?

The FDA product code for INFUTROL 7000 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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