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ENDOSCOPIC ELECTROSURGICAL FIBEROPTIC PROBE

Page Type
Cleared 510(K)
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)
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