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ENDOSCOPIC ELECTROSURGICAL FIBEROPTIC PROBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861331
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1986
Days to Decision
120 days

ENDOSCOPIC ELECTROSURGICAL FIBEROPTIC PROBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861331
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1986
Days to Decision
120 days