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GENII ARC SMART ARGON PROBE

Page Type
Cleared 510(K)
510(k) Number
K130983
510(k) Type
Traditional
Applicant
GENII, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2013
Days to Decision
170 days
Submission Type
Summary

GENII ARC SMART ARGON PROBE

Page Type
Cleared 510(K)
510(k) Number
K130983
510(k) Type
Traditional
Applicant
GENII, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2013
Days to Decision
170 days
Submission Type
Summary