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FDA 510(k)

A SERIES OF 7 INCH CONTINUOUS INFUSION SETS

K-Number: K874403 · 1987-12-29

ApplicantQuinton, Inc.
Decision Date1987-12-29
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

A SERIES OF 7 INCH CONTINUOUS INFUSION SETS is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1987-12-29 under 510(k) number K874403. 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 A SERIES OF 7 INCH CONTINUOUS INFUSION SETS?

A SERIES OF 7 INCH CONTINUOUS INFUSION SETS is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Quinton, Inc.. The 510(k) number is K874403.

When did A SERIES OF 7 INCH CONTINUOUS INFUSION SETS receive FDA 510(k) clearance?

A SERIES OF 7 INCH CONTINUOUS INFUSION SETS received FDA 510(k) clearance on 1987-12-29, under 510(k) number K874403.

Who is the listed applicant for A SERIES OF 7 INCH CONTINUOUS INFUSION SETS?

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

What is the FDA product code for A SERIES OF 7 INCH CONTINUOUS INFUSION SETS?

The FDA product code for A SERIES OF 7 INCH CONTINUOUS INFUSION SETS 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 Quinton, 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 164 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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