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COAGULATION ELECTRODE, MODEL 2000; RADIOFREQUENCY GENERATOR, MODEL 20-115

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993900
510(k) Type
Traditional
Applicant
BRONCUS TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2000
Days to Decision
73 days
Submission Type
Summary

COAGULATION ELECTRODE, MODEL 2000; RADIOFREQUENCY GENERATOR, MODEL 20-115

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993900
510(k) Type
Traditional
Applicant
BRONCUS TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2000
Days to Decision
73 days
Submission Type
Summary