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FDA 510(k)

ABBOTT PLUM A+ INFUSION PUMP

K-Number: K982159 · 1999-01-12

ApplicantAbbott Laboratories
Decision Date1999-01-12
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ABBOTT PLUM A+ 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 1999-01-12 under 510(k) number K982159. 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 ABBOTT PLUM A+ INFUSION PUMP?

ABBOTT PLUM A+ INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1999-01-12. The listed applicant is Abbott Laboratories. The 510(k) number is K982159.

When did ABBOTT PLUM A+ INFUSION PUMP receive FDA 510(k) clearance?

ABBOTT PLUM A+ INFUSION PUMP received FDA 510(k) clearance on 1999-01-12, under 510(k) number K982159.

Who is the listed applicant for ABBOTT PLUM A+ 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 ABBOTT PLUM A+ INFUSION PUMP?

The FDA product code for ABBOTT PLUM A+ 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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