Atlas FDA

LifeGlobal Micro Tips

FDA 510(k) clearance K152581 · decided 2016-04-11

Clearance details

K-number
K152581
Device name
LifeGlobal Micro Tips
Applicant
Life Global Group, LLC
Decision
Substantially Equivalent
Date received
2015-09-10
Decision date
2016-04-11
Days to decision
214 days
Clearance type
Traditional
Product code
MQH
Device class
2
Regulation number
884.6130
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Gilford, CT, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.