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FDA 510(k)

MODEL 3000 INFUSION PUMP

K-Number: K871881 · 1988-01-06

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1988-01-06
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 3000 INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1988-01-06 under 510(k) number K871881. 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 3000 INFUSION PUMP?

MODEL 3000 INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1988-01-06. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K871881.

When did MODEL 3000 INFUSION PUMP receive FDA 510(k) clearance?

MODEL 3000 INFUSION PUMP received FDA 510(k) clearance on 1988-01-06, under 510(k) number K871881.

Who is the listed applicant for MODEL 3000 INFUSION PUMP?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 3000 INFUSION PUMP?

The FDA product code for MODEL 3000 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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