FDA 510(k)

LifeGlobal Micro Tips

K-Number: K152581 · 2016-04-11

Decision Date2016-04-11

Product CodeMQH

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

LifeGlobal Micro Tips is the device name listed in this FDA 510(k) record. The listed applicant is Life Global Group, LLC. It received FDA 510(k) clearance on 2016-04-11 under 510(k) number K152581. The device is classified under product code MQH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LifeGlobal Micro Tips?

LifeGlobal Micro Tips is a medical device that received FDA 510(k) clearance on 2016-04-11. The listed applicant is Life Global Group, LLC. The 510(k) number is K152581.

When did LifeGlobal Micro Tips receive FDA 510(k) clearance?

LifeGlobal Micro Tips received FDA 510(k) clearance on 2016-04-11, under 510(k) number K152581.

Who is the listed applicant for LifeGlobal Micro Tips?

The FDA 510(k) record lists Life Global Group, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LifeGlobal Micro Tips?

The FDA product code for LifeGlobal Micro Tips is MQH.

Related Devices (Code: MQH)

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.

K250838Denudation PipettesGuangzhou Pinzhi Medical Device Co., Ltd.K192146V-DENUPETVitromed GmbH K161275EZ-Tip Singles, EZ-Tip Vial of 20, EZ-GripResearch Instruments Limited K151018Embryo Biopsy Pipette, Polar Body Biopsy Pipette, Testicular Sperm Extraction PipetteCook Incorporated

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.