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FDA 510(k)

INFUSION EQUIPMENT, INTRAVENOUS

K-Number: K760370 · 1976-08-23

ApplicantValleylab, Inc.
Decision Date1976-08-23
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFUSION EQUIPMENT, INTRAVENOUS is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1976-08-23 under 510(k) number K760370. 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 INFUSION EQUIPMENT, INTRAVENOUS?

INFUSION EQUIPMENT, INTRAVENOUS is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is Valleylab, Inc.. The 510(k) number is K760370.

When did INFUSION EQUIPMENT, INTRAVENOUS receive FDA 510(k) clearance?

INFUSION EQUIPMENT, INTRAVENOUS received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760370.

Who is the listed applicant for INFUSION EQUIPMENT, INTRAVENOUS?

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 INFUSION EQUIPMENT, INTRAVENOUS?

The FDA product code for INFUSION EQUIPMENT, INTRAVENOUS 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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