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FDA 510(k)

RATE INFUSER PLUS

K-Number: K900742 · 1990-07-11

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1990-07-11
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RATE INFUSER PLUS 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 1990-07-11 under 510(k) number K900742. 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 RATE INFUSER PLUS?

RATE INFUSER PLUS is a medical device that received FDA 510(k) clearance on 1990-07-11. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K900742.

When did RATE INFUSER PLUS receive FDA 510(k) clearance?

RATE INFUSER PLUS received FDA 510(k) clearance on 1990-07-11, under 510(k) number K900742.

Who is the listed applicant for RATE INFUSER PLUS?

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 RATE INFUSER PLUS?

The FDA product code for RATE INFUSER PLUS 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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