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FDA 510(k)

AVI MODEL 3100 INFUSION PUMP

K-Number: K923068 · 1993-04-20

Applicant3M Health Care, Ltd.
Decision Date1993-04-20
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AVI MODEL 3100 INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Ltd.. It received FDA 510(k) clearance on 1993-04-20 under 510(k) number K923068. 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 AVI MODEL 3100 INFUSION PUMP?

AVI MODEL 3100 INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is 3M Health Care, Ltd.. The 510(k) number is K923068.

When did AVI MODEL 3100 INFUSION PUMP receive FDA 510(k) clearance?

AVI MODEL 3100 INFUSION PUMP received FDA 510(k) clearance on 1993-04-20, under 510(k) number K923068.

Who is the listed applicant for AVI MODEL 3100 INFUSION PUMP?

The FDA 510(k) record lists 3M Health Care, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AVI MODEL 3100 INFUSION PUMP?

The FDA product code for AVI MODEL 3100 INFUSION PUMP is FRN.

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Related Devices (Code: 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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