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FDA 510(k)

RATEMINDER V INFUSION PUMP W/SECONDARY CAPABILITY

K-Number: K902092 · 1990-07-26

ApplicantCritikon Company, LLC
Decision Date1990-07-26
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RATEMINDER V INFUSION PUMP W/SECONDARY CAPABILITY 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 1990-07-26 under 510(k) number K902092. 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 W/SECONDARY CAPABILITY?

RATEMINDER V INFUSION PUMP W/SECONDARY CAPABILITY is a medical device that received FDA 510(k) clearance on 1990-07-26. The listed applicant is Critikon Company, LLC. The 510(k) number is K902092.

When did RATEMINDER V INFUSION PUMP W/SECONDARY CAPABILITY receive FDA 510(k) clearance?

RATEMINDER V INFUSION PUMP W/SECONDARY CAPABILITY received FDA 510(k) clearance on 1990-07-26, under 510(k) number K902092.

Who is the listed applicant for RATEMINDER V INFUSION PUMP W/SECONDARY CAPABILITY?

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 W/SECONDARY CAPABILITY?

The FDA product code for RATEMINDER V INFUSION PUMP W/SECONDARY CAPABILITY 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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