Last synced on 27 January 2023 at 11:04 pm

OCULOSTAT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981235
510(k) Type
Traditional
Applicant
LASER CENTER DEV. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/1998
Days to Decision
103 days
Submission Type
Summary

OCULOSTAT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981235
510(k) Type
Traditional
Applicant
LASER CENTER DEV. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/1998
Days to Decision
103 days
Submission Type
Summary