FDA 510(k)

HARVARD APPARATUS INTERMITTENT INFUSION

K-Number: K830102 · 1983-02-28

Decision Date1983-02-28

Product CodeFRN

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

HARVARD APPARATUS INTERMITTENT INFUSION 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 1983-02-28 under 510(k) number K830102. 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 INTERMITTENT INFUSION?

HARVARD APPARATUS INTERMITTENT INFUSION is a medical device that received FDA 510(k) clearance on 1983-02-28. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K830102.

When did HARVARD APPARATUS INTERMITTENT INFUSION receive FDA 510(k) clearance?

HARVARD APPARATUS INTERMITTENT INFUSION received FDA 510(k) clearance on 1983-02-28, under 510(k) number K830102.

Who is the listed applicant for HARVARD APPARATUS INTERMITTENT INFUSION?

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 INTERMITTENT INFUSION?

The FDA product code for HARVARD APPARATUS INTERMITTENT INFUSION 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.