Last synced on 6 June 2025 at 11:06 pm

TRIMEDYNE MODEL 1210 OMNIPULSE HOLMIUM LASE SYST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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