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MODEL 1210 OMNIPULSE HOLMIUM LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K915117
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/1992
Days to Decision
141 days
Submission Type
Statement

MODEL 1210 OMNIPULSE HOLMIUM LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K915117
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/1992
Days to Decision
141 days
Submission Type
Statement