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FDA 510(k)

4 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMP

K-Number: K905218 · 1991-06-04

Decision Date1991-06-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

4 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMP 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 1991-06-04 under 510(k) number K905218. 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 4 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMP?

4 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMP is a medical device that received FDA 510(k) clearance on 1991-06-04. The listed applicant is Marquette Medical, Inc.. The 510(k) number is K905218.

When did 4 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMP receive FDA 510(k) clearance?

4 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMP received FDA 510(k) clearance on 1991-06-04, under 510(k) number K905218.

Who is the listed applicant for 4 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMP?

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 4 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMP?

The FDA product code for 4 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMP 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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