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FDA 510(k)

JIERUI SYRINGES AND NEEDLES

K-Number: K072739 · 2008-03-21

Decision Date2008-03-21
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

JIERUI SYRINGES AND NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Shandong Weigao Group Medical Polymer Co., Ltd.. It received FDA 510(k) clearance on 2008-03-21 under 510(k) number K072739. 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 JIERUI SYRINGES AND NEEDLES?

JIERUI SYRINGES AND NEEDLES is a medical device that received FDA 510(k) clearance on 2008-03-21. The listed applicant is Shandong Weigao Group Medical Polymer Co., Ltd.. The 510(k) number is K072739.

When did JIERUI SYRINGES AND NEEDLES receive FDA 510(k) clearance?

JIERUI SYRINGES AND NEEDLES received FDA 510(k) clearance on 2008-03-21, under 510(k) number K072739.

Who is the listed applicant for JIERUI SYRINGES AND NEEDLES?

The FDA 510(k) record lists Shandong Weigao Group Medical Polymer Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JIERUI SYRINGES AND NEEDLES?

The FDA product code for JIERUI SYRINGES AND NEEDLES 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.

Other records listing Shandong Weigao Group Medical Polymer Co., Ltd. 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 7 devices →

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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