Last synced on 23 September 2022 at 11:05 pm

OPACITRAC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915356
510(k) Type
Traditional
Applicant
OCULON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1992
Days to Decision
87 days
Submission Type
Statement

OPACITRAC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915356
510(k) Type
Traditional
Applicant
OCULON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1992
Days to Decision
87 days
Submission Type
Statement