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FDA 510(k)

AR/MDE INFUSOR MODEL 60/2 INFUSION PUMP

K-Number: K791720 · 1979-11-05

ApplicantAlza Corp.
Decision Date1979-11-05
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AR/MDE INFUSOR MODEL 60/2 INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Alza Corp.. It received FDA 510(k) clearance on 1979-11-05 under 510(k) number K791720. 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 AR/MDE INFUSOR MODEL 60/2 INFUSION PUMP?

AR/MDE INFUSOR MODEL 60/2 INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1979-11-05. The listed applicant is Alza Corp.. The 510(k) number is K791720.

When did AR/MDE INFUSOR MODEL 60/2 INFUSION PUMP receive FDA 510(k) clearance?

AR/MDE INFUSOR MODEL 60/2 INFUSION PUMP received FDA 510(k) clearance on 1979-11-05, under 510(k) number K791720.

Who is the listed applicant for AR/MDE INFUSOR MODEL 60/2 INFUSION PUMP?

The FDA 510(k) record lists Alza Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AR/MDE INFUSOR MODEL 60/2 INFUSION PUMP?

The FDA product code for AR/MDE INFUSOR MODEL 60/2 INFUSION PUMP is FRN.

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Related Devices (Code: FRN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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