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510k Database
Manufacturers
US
Thermedical
Medical Device Manufacturer
·
US , Philedelphia , PA
Thermedical - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2012
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Thermedical
General & Plastic Surgery
✕
1
devices
1-1 of 1
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Cleared
Oct 01, 2012
SERF ABLATION SYSTEM SERF ABLATION NEEDLE
K120116
·
GEI
General & Plastic Surgery
·
262d
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General & Plastic Surgery
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