Last synced on 14 November 2025 at 11:06 pm

OPTILASE MODEL 1000 ND:YAG LASER ADD'L INDICATION

Page Type
Cleared 510(K)
510(k) Number
K902263
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1990
Days to Decision
63 days

OPTILASE MODEL 1000 ND:YAG LASER ADD'L INDICATION

Page Type
Cleared 510(K)
510(k) Number
K902263
510(k) Type
Traditional
Applicant
TRIMEDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1990
Days to Decision
63 days