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FDA 510(k)

CLICKZIP, MODEL U-100 INSULIN SAFETY SYRINGE

K-Number: K062780 · 2007-01-05

Decision Date2007-01-05
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CLICKZIP, MODEL U-100 INSULIN SAFETY SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Manufacturer (Thailand) , Ltd.. It received FDA 510(k) clearance on 2007-01-05 under 510(k) number K062780. 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 CLICKZIP, MODEL U-100 INSULIN SAFETY SYRINGE?

CLICKZIP, MODEL U-100 INSULIN SAFETY SYRINGE is a medical device that received FDA 510(k) clearance on 2007-01-05. The listed applicant is Medical Device Manufacturer (Thailand) , Ltd.. The 510(k) number is K062780.

When did CLICKZIP, MODEL U-100 INSULIN SAFETY SYRINGE receive FDA 510(k) clearance?

CLICKZIP, MODEL U-100 INSULIN SAFETY SYRINGE received FDA 510(k) clearance on 2007-01-05, under 510(k) number K062780.

Who is the listed applicant for CLICKZIP, MODEL U-100 INSULIN SAFETY SYRINGE?

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

What is the FDA product code for CLICKZIP, MODEL U-100 INSULIN SAFETY SYRINGE?

The FDA product code for CLICKZIP, MODEL U-100 INSULIN SAFETY SYRINGE 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 Medical Device Manufacturer (Thailand) , 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.

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