Last synced on 30 September 2022 at 11:05 pm

OPTEC 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924741
510(k) Type
Traditional
Applicant
STEREO OPTICAL CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1993
Days to Decision
196 days
Submission Type
Statement

OPTEC 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924741
510(k) Type
Traditional
Applicant
STEREO OPTICAL CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1993
Days to Decision
196 days
Submission Type
Statement