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CERULEAU ELECTROSURGICAL PROBE

Page Type
Cleared 510(K)
510(k) Number
K101711
510(k) Type
Traditional
Applicant
NUORTHO SURGICAL, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2010
Days to Decision
13 days
Submission Type
Summary

CERULEAU ELECTROSURGICAL PROBE

Page Type
Cleared 510(K)
510(k) Number
K101711
510(k) Type
Traditional
Applicant
NUORTHO SURGICAL, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2010
Days to Decision
13 days
Submission Type
Summary