Last synced on 30 September 2022 at 11:05 pm

TBD KERATOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912130
510(k) Type
Traditional
Applicant
ALCON LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1991
Days to Decision
87 days
Submission Type
Statement

TBD KERATOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912130
510(k) Type
Traditional
Applicant
ALCON LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1991
Days to Decision
87 days
Submission Type
Statement