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FDA 510(k)

YUE PFONG SAFETY SYRINGE (3ML)

K-Number: K040105 · 2004-04-07

Decision Date2004-04-07
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

YUE PFONG SAFETY SYRINGE (3ML) is the device name listed in this FDA 510(k) record. The listed applicant is Yue Pfong International Industrial Co., Ltd.. It received FDA 510(k) clearance on 2004-04-07 under 510(k) number K040105. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YUE PFONG SAFETY SYRINGE (3ML)?

YUE PFONG SAFETY SYRINGE (3ML) is a medical device that received FDA 510(k) clearance on 2004-04-07. The listed applicant is Yue Pfong International Industrial Co., Ltd.. The 510(k) number is K040105.

When did YUE PFONG SAFETY SYRINGE (3ML) receive FDA 510(k) clearance?

YUE PFONG SAFETY SYRINGE (3ML) received FDA 510(k) clearance on 2004-04-07, under 510(k) number K040105.

Who is the listed applicant for YUE PFONG SAFETY SYRINGE (3ML)?

The FDA 510(k) record lists Yue Pfong International Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YUE PFONG SAFETY SYRINGE (3ML)?

The FDA product code for YUE PFONG SAFETY SYRINGE (3ML) is MEG.

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: MEG)

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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