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LAPAROSCOPIC RESECTION DEVICE, MODEL SR326L

Page Type
Cleared 510(K)
510(k) Number
K091440
510(k) Type
Traditional
Applicant
Bovie Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2009
Days to Decision
147 days
Submission Type
Summary

LAPAROSCOPIC RESECTION DEVICE, MODEL SR326L

Page Type
Cleared 510(K)
510(k) Number
K091440
510(k) Type
Traditional
Applicant
Bovie Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2009
Days to Decision
147 days
Submission Type
Summary