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FDA 510(k)

RATEMINDER(TM) V INFUSION PUMP, MODIFICATION

K-Number: K911769 · 1991-06-03

ApplicantCritikon Company, LLC
Decision Date1991-06-03
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RATEMINDER(TM) V INFUSION PUMP, MODIFICATION 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 1991-06-03 under 510(k) number K911769. 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(TM) V INFUSION PUMP, MODIFICATION?

RATEMINDER(TM) V INFUSION PUMP, MODIFICATION is a medical device that received FDA 510(k) clearance on 1991-06-03. The listed applicant is Critikon Company, LLC. The 510(k) number is K911769.

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

RATEMINDER(TM) V INFUSION PUMP, MODIFICATION received FDA 510(k) clearance on 1991-06-03, under 510(k) number K911769.

Who is the listed applicant for RATEMINDER(TM) V INFUSION PUMP, MODIFICATION?

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(TM) V INFUSION PUMP, MODIFICATION?

The FDA product code for RATEMINDER(TM) V INFUSION PUMP, MODIFICATION is FRN.

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Other records listing Critikon Company, LLC as applicant

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Related Devices (Code: FRN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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