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FDA 510(k)

PLUM XL INFUSION PUMP

K-Number: K944733 · 1995-02-08

ApplicantAbbott Laboratories
Decision Date1995-02-08
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

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 1995-02-08 under 510(k) number K944733. 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 PLUM XL INFUSION PUMP?

PLUM XL INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1995-02-08. The listed applicant is Abbott Laboratories. The 510(k) number is K944733.

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

PLUM XL INFUSION PUMP received FDA 510(k) clearance on 1995-02-08, under 510(k) number K944733.

Who is the listed applicant for 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 PLUM XL INFUSION PUMP?

The FDA product code for 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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