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ELECTROSURGICAL CAUTERY PROBES

Page Type
Cleared 510(K)
510(k) Number
K981188
510(k) Type
Traditional
Applicant
MICROLINE PENTAX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1998
Days to Decision
48 days
Submission Type
Summary

ELECTROSURGICAL CAUTERY PROBES

Page Type
Cleared 510(K)
510(k) Number
K981188
510(k) Type
Traditional
Applicant
MICROLINE PENTAX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1998
Days to Decision
48 days
Submission Type
Summary