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FDA 510(k)

LOW VOLUME TRIFURCATED IV EXTENSION SET

K-Number: K901089 · 1990-10-04

Decision Date1990-10-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LOW VOLUME TRIFURCATED IV EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Medical, Inc.. It received FDA 510(k) clearance on 1990-10-04 under 510(k) number K901089. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOW VOLUME TRIFURCATED IV EXTENSION SET?

LOW VOLUME TRIFURCATED IV EXTENSION SET is a medical device that received FDA 510(k) clearance on 1990-10-04. The listed applicant is Marquette Medical, Inc.. The 510(k) number is K901089.

When did LOW VOLUME TRIFURCATED IV EXTENSION SET receive FDA 510(k) clearance?

LOW VOLUME TRIFURCATED IV EXTENSION SET received FDA 510(k) clearance on 1990-10-04, under 510(k) number K901089.

Who is the listed applicant for LOW VOLUME TRIFURCATED IV EXTENSION SET?

The FDA 510(k) record lists Marquette Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOW VOLUME TRIFURCATED IV EXTENSION SET?

The FDA product code for LOW VOLUME TRIFURCATED IV EXTENSION SET is FPA.

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.

Other records listing Marquette Medical, Inc. as applicant

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.

View all 17 devices →

Related Devices (Code: FPA)

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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