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Shannon Group
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K820156
THEIR ELECTRO SURGICAL COUTERY PENCIL
February 18, 1982
K811205
MOLDED POLYSULFONE TRIAL PROSTHESIS
May 21, 1981