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FDA 510(k)

VITAL INFUSION PUMP

K-Number: K914122 · 1992-09-03

Decision Date1992-09-03
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITAL INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Vital Resources Corp.. It received FDA 510(k) clearance on 1992-09-03 under 510(k) number K914122. 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 VITAL INFUSION PUMP?

VITAL INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1992-09-03. The listed applicant is Vital Resources Corp.. The 510(k) number is K914122.

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

VITAL INFUSION PUMP received FDA 510(k) clearance on 1992-09-03, under 510(k) number K914122.

Who is the listed applicant for VITAL INFUSION PUMP?

The FDA 510(k) record lists Vital Resources Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITAL INFUSION PUMP?

The FDA product code for VITAL INFUSION PUMP is FRN.

Related Clinical Trials

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.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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