Last synced on 27 January 2023 at 11:04 pm

OCULAB TONOPEN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852774
510(k) Type
Traditional
Applicant
OCULAB, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1985
Days to Decision
50 days

OCULAB TONOPEN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852774
510(k) Type
Traditional
Applicant
OCULAB, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1985
Days to Decision
50 days