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FDA 510(k)

DISPOSABLE INFUSION SET

K-Number: K090012 · 2009-06-11

Decision Date2009-06-11
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Shan Dong Wei Gao Group Medical Polymer Products. It received FDA 510(k) clearance on 2009-06-11 under 510(k) number K090012. 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 DISPOSABLE INFUSION SET?

DISPOSABLE INFUSION SET is a medical device that received FDA 510(k) clearance on 2009-06-11. The listed applicant is Shan Dong Wei Gao Group Medical Polymer Products. The 510(k) number is K090012.

When did DISPOSABLE INFUSION SET receive FDA 510(k) clearance?

DISPOSABLE INFUSION SET received FDA 510(k) clearance on 2009-06-11, under 510(k) number K090012.

Who is the listed applicant for DISPOSABLE INFUSION SET?

The FDA 510(k) record lists Shan Dong Wei Gao Group Medical Polymer Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE INFUSION SET?

The FDA product code for DISPOSABLE INFUSION 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 Shan Dong Wei Gao Group Medical Polymer Products 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.

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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