Atlas FDA

DISPOSABLE ENDOSCOPIC CANNULA

FDA 510(k) clearance K140213 · decided 2015-03-25

Clearance details

K-number
K140213
Device name
DISPOSABLE ENDOSCOPIC CANNULA
Applicant
Dongguan Microview Medical Technology Co., Ltd.
Decision
Substantially Equivalent
Date received
2014-01-28
Decision date
2015-03-25
Days to decision
421 days
Clearance type
Traditional
Product code
HGH
Device class
2
Regulation number
884.5070
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Shenzhen, Guangdong, CN
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.