510(k) K222225

Device
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Applicant
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510(k) number
K222225
Product code
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Decision
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Decision date
2022-11-11
Date received
2022-07-25
Regulation
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Classification name
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Medical specialty
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Review panel
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Device class
1
Clearance type
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Statement or summary
Summary
Third party reviewed
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Applicant Contact#

Contact
Kuan Mun Leong
Address
# 1, Persiaran Tanjung, Kawasan Perindustrian Tanjung Sepang MY 43900 43900

FDA Registration Numbers#

Source Documents#

510(k) summary PDF