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FDA 510(k)

HEPARIN INFUSIN PUMP

K-Number: K843878 · 1984-12-06

ApplicantArmament Systems, Inc.
Decision Date1984-12-06
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HEPARIN INFUSIN PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Armament Systems, Inc.. It received FDA 510(k) clearance on 1984-12-06 under 510(k) number K843878. 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 HEPARIN INFUSIN PUMP?

HEPARIN INFUSIN PUMP is a medical device that received FDA 510(k) clearance on 1984-12-06. The listed applicant is Armament Systems, Inc.. The 510(k) number is K843878.

When did HEPARIN INFUSIN PUMP receive FDA 510(k) clearance?

HEPARIN INFUSIN PUMP received FDA 510(k) clearance on 1984-12-06, under 510(k) number K843878.

Who is the listed applicant for HEPARIN INFUSIN PUMP?

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

What is the FDA product code for HEPARIN INFUSIN PUMP?

The FDA product code for HEPARIN INFUSIN PUMP 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.

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