FDA 510(k)

HARVARD APPARATUS FAMILY OF FLUID INFUS

K-Number: K830177 · 1983-02-07

Decision Date1983-02-07

Product CodeFRN

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

HARVARD APPARATUS FAMILY OF FLUID INFUS is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1983-02-07 under 510(k) number K830177. 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 HARVARD APPARATUS FAMILY OF FLUID INFUS?

HARVARD APPARATUS FAMILY OF FLUID INFUS is a medical device that received FDA 510(k) clearance on 1983-02-07. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K830177.

When did HARVARD APPARATUS FAMILY OF FLUID INFUS receive FDA 510(k) clearance?

HARVARD APPARATUS FAMILY OF FLUID INFUS received FDA 510(k) clearance on 1983-02-07, under 510(k) number K830177.

Who is the listed applicant for HARVARD APPARATUS FAMILY OF FLUID INFUS?

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

What is the FDA product code for HARVARD APPARATUS FAMILY OF FLUID INFUS?

The FDA product code for HARVARD APPARATUS FAMILY OF FLUID INFUS is FRN.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.