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FDA 510(k)

MODIFICATION TO PLUM XL INFUSION PUMP

K-Number: K010924 · 2001-04-06

ApplicantAbbott Laboratories
Decision Date2001-04-06
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO PLUM XL INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 2001-04-06 under 510(k) number K010924. 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 MODIFICATION TO PLUM XL INFUSION PUMP?

MODIFICATION TO PLUM XL INFUSION PUMP is a medical device that received FDA 510(k) clearance on 2001-04-06. The listed applicant is Abbott Laboratories. The 510(k) number is K010924.

When did MODIFICATION TO PLUM XL INFUSION PUMP receive FDA 510(k) clearance?

MODIFICATION TO PLUM XL INFUSION PUMP received FDA 510(k) clearance on 2001-04-06, under 510(k) number K010924.

Who is the listed applicant for MODIFICATION TO PLUM XL INFUSION PUMP?

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

What is the FDA product code for MODIFICATION TO PLUM XL INFUSION PUMP?

The FDA product code for MODIFICATION TO PLUM XL INFUSION PUMP is 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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