Last synced on 14 November 2025 at 11:06 pm

ESTILUX POSTERIOR XR

Page Type
Cleared 510(K)
510(k) Number
K813568
510(k) Type
Traditional
Applicant
KULZER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1982
Days to Decision
38 days

ESTILUX POSTERIOR XR

Page Type
Cleared 510(K)
510(k) Number
K813568
510(k) Type
Traditional
Applicant
KULZER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1982
Days to Decision
38 days