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SALINE ENHANCED ELECTROSURGICAL RESECTION (SEER) DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082568
510(k) Type
Traditional
Applicant
BOVIE MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2008
Days to Decision
74 days
Submission Type
Summary

SALINE ENHANCED ELECTROSURGICAL RESECTION (SEER) DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082568
510(k) Type
Traditional
Applicant
BOVIE MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2008
Days to Decision
74 days
Submission Type
Summary