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TRIMEDYNE MODEL 1210 OMNIPULSE HOLMIUM LASER SYST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922496
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1994
Days to Decision
643 days
Submission Type
Statement

TRIMEDYNE MODEL 1210 OMNIPULSE HOLMIUM LASER SYST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922496
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1994
Days to Decision
643 days
Submission Type
Statement