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LATERALASE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K925414
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1994
Days to Decision
491 days
Submission Type
Statement

LATERALASE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K925414
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1994
Days to Decision
491 days
Submission Type
Statement