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BOSS COAGULATION DEVICE, MODEL BOSS1215, BOSS COAGULATION DEVICE, ANGLED ACCESS, MODEL BOSA1215

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092149
510(k) Type
Traditional
Applicant
Bovie Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/2010
Days to Decision
245 days
Submission Type
Summary

BOSS COAGULATION DEVICE, MODEL BOSS1215, BOSS COAGULATION DEVICE, ANGLED ACCESS, MODEL BOSA1215

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092149
510(k) Type
Traditional
Applicant
Bovie Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/2010
Days to Decision
245 days
Submission Type
Summary