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FDA 510(k)

ABBOTT ACCLAIM ENCORE STANDARD TUBING PUMP

K-Number: K002126 · 2000-07-20

ApplicantAbbott Laboratories
Decision Date2000-07-20
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ABBOTT ACCLAIM ENCORE STANDARD TUBING 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 2000-07-20 under 510(k) number K002126. 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 ACCLAIM ENCORE STANDARD TUBING PUMP?

ABBOTT ACCLAIM ENCORE STANDARD TUBING PUMP is a medical device that received FDA 510(k) clearance on 2000-07-20. The listed applicant is Abbott Laboratories. The 510(k) number is K002126.

When did ABBOTT ACCLAIM ENCORE STANDARD TUBING PUMP receive FDA 510(k) clearance?

ABBOTT ACCLAIM ENCORE STANDARD TUBING PUMP received FDA 510(k) clearance on 2000-07-20, under 510(k) number K002126.

Who is the listed applicant for ABBOTT ACCLAIM ENCORE STANDARD TUBING 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 ACCLAIM ENCORE STANDARD TUBING PUMP?

The FDA product code for ABBOTT ACCLAIM ENCORE STANDARD TUBING 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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