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TRIMEDYNE MODEL 1210 OMNIPULSE HOLMIUM LASE SYST

Page Type
Cleared 510(K)
510(k) Number
K925124
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1994
Days to Decision
504 days
Submission Type
Statement

TRIMEDYNE MODEL 1210 OMNIPULSE HOLMIUM LASE SYST

Page Type
Cleared 510(K)
510(k) Number
K925124
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1994
Days to Decision
504 days
Submission Type
Statement