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FDA 510(k)

MODEL 885 INFUSION PUMP, MODIFICATION

K-Number: K924872 · 1993-06-17

Applicant3M Health Care, Ltd.
Decision Date1993-06-17
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 885 INFUSION PUMP, MODIFICATION 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 1993-06-17 under 510(k) number K924872. 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 MODEL 885 INFUSION PUMP, MODIFICATION?

MODEL 885 INFUSION PUMP, MODIFICATION is a medical device that received FDA 510(k) clearance on 1993-06-17. The listed applicant is 3M Health Care, Ltd.. The 510(k) number is K924872.

When did MODEL 885 INFUSION PUMP, MODIFICATION receive FDA 510(k) clearance?

MODEL 885 INFUSION PUMP, MODIFICATION received FDA 510(k) clearance on 1993-06-17, under 510(k) number K924872.

Who is the listed applicant for MODEL 885 INFUSION PUMP, MODIFICATION?

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 MODEL 885 INFUSION PUMP, MODIFICATION?

The FDA product code for MODEL 885 INFUSION PUMP, MODIFICATION 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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