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FDA 510(k)

RATEMINDER V INFUSION PUMP

K-Number: K875174 · 1988-03-29

ApplicantCritikon Company, LLC
Decision Date1988-03-29
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RATEMINDER V INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Critikon Company, LLC. It received FDA 510(k) clearance on 1988-03-29 under 510(k) number K875174. 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 RATEMINDER V INFUSION PUMP?

RATEMINDER V INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1988-03-29. The listed applicant is Critikon Company, LLC. The 510(k) number is K875174.

When did RATEMINDER V INFUSION PUMP receive FDA 510(k) clearance?

RATEMINDER V INFUSION PUMP received FDA 510(k) clearance on 1988-03-29, under 510(k) number K875174.

Who is the listed applicant for RATEMINDER V INFUSION PUMP?

The FDA 510(k) record lists Critikon Company, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RATEMINDER V INFUSION PUMP?

The FDA product code for RATEMINDER V 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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