Last synced on 25 April 2025 at 11:05 pm

MODEL 1210 OMNIPULSE HOLMIUM LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914952
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1991
Days to Decision
45 days
Submission Type
Statement

MODEL 1210 OMNIPULSE HOLMIUM LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914952
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1991
Days to Decision
45 days
Submission Type
Statement