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FDA 510(k)

UNIQSAFE ROTATABLE, RETRACTABLE SAFETY SYRINGES

K-Number: K050116 · 2005-05-09

ApplicantUniqsafe Biomeditech Co., Ltd.
Decision Date2005-05-09
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNIQSAFE ROTATABLE, RETRACTABLE SAFETY SYRINGES is the device name listed in this FDA 510(k) record. The listed applicant is Uniqsafe Biomeditech Co., Ltd.. It received FDA 510(k) clearance on 2005-05-09 under 510(k) number K050116. 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 UNIQSAFE ROTATABLE, RETRACTABLE SAFETY SYRINGES?

UNIQSAFE ROTATABLE, RETRACTABLE SAFETY SYRINGES is a medical device that received FDA 510(k) clearance on 2005-05-09. The listed applicant is Uniqsafe Biomeditech Co., Ltd.. The 510(k) number is K050116.

When did UNIQSAFE ROTATABLE, RETRACTABLE SAFETY SYRINGES receive FDA 510(k) clearance?

UNIQSAFE ROTATABLE, RETRACTABLE SAFETY SYRINGES received FDA 510(k) clearance on 2005-05-09, under 510(k) number K050116.

Who is the listed applicant for UNIQSAFE ROTATABLE, RETRACTABLE SAFETY SYRINGES?

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

What is the FDA product code for UNIQSAFE ROTATABLE, RETRACTABLE SAFETY SYRINGES?

The FDA product code for UNIQSAFE ROTATABLE, RETRACTABLE SAFETY SYRINGES is MEG.

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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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