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Kronos Electrocautery Device

Page Type
Cleared 510(K)
510(k) Number
K232805
510(k) Type
Traditional
Applicant
Single Pass, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2024
Days to Decision
226 days
Submission Type
Summary

Kronos Electrocautery Device

Page Type
Cleared 510(K)
510(k) Number
K232805
510(k) Type
Traditional
Applicant
Single Pass, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2024
Days to Decision
226 days
Submission Type
Summary