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FDA 510(k)

Jeesung Safety Syringe and Single Use Needles

K-Number: K152606 · 2016-06-28

Decision Date2016-06-28
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Jeesung Safety Syringe and Single Use Needles is the device name listed in this FDA 510(k) record. The listed applicant is Jeesung Medical Co., Ltd.. It received FDA 510(k) clearance on 2016-06-28 under 510(k) number K152606. 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 Jeesung Safety Syringe and Single Use Needles?

Jeesung Safety Syringe and Single Use Needles is a medical device that received FDA 510(k) clearance on 2016-06-28. The listed applicant is Jeesung Medical Co., Ltd.. The 510(k) number is K152606.

When did Jeesung Safety Syringe and Single Use Needles receive FDA 510(k) clearance?

Jeesung Safety Syringe and Single Use Needles received FDA 510(k) clearance on 2016-06-28, under 510(k) number K152606.

Who is the listed applicant for Jeesung Safety Syringe and Single Use Needles?

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

What is the FDA product code for Jeesung Safety Syringe and Single Use Needles?

The FDA product code for Jeesung Safety Syringe and Single Use 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 Jeesung Medical 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.

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.