Last synced on 27 January 2023 at 11:04 pm

RETINADX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003236
510(k) Type
Traditional
Applicant
REGULATORY ASSOCIATES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2000
Days to Decision
16 days
Submission Type
Statement

RETINADX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003236
510(k) Type
Traditional
Applicant
REGULATORY ASSOCIATES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2000
Days to Decision
16 days
Submission Type
Statement