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ULTRACLEAN HANDCONTROLLED SUCTION COAGULATOR, MODEL 130182, 130183, 130184, 130185; ULTRACLEAN FOOTCONTROLLED SUCTION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052104
510(k) Type
Traditional
Applicant
CONMED CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2005
Days to Decision
79 days
Submission Type
Summary

ULTRACLEAN HANDCONTROLLED SUCTION COAGULATOR, MODEL 130182, 130183, 130184, 130185; ULTRACLEAN FOOTCONTROLLED SUCTION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052104
510(k) Type
Traditional
Applicant
CONMED CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2005
Days to Decision
79 days
Submission Type
Summary