Last synced on 23 September 2022 at 11:05 pm

D.L. SCOPE OPHTHALMOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896072
510(k) Type
Traditional
Applicant
NORTH AMERICAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1989
Days to Decision
39 days

D.L. SCOPE OPHTHALMOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896072
510(k) Type
Traditional
Applicant
NORTH AMERICAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1989
Days to Decision
39 days