Last synced on 27 January 2023 at 11:04 pm

SEIKO P-2 & SEIKO P-3 (SPECTACLE LENS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861684
510(k) Type
Traditional
Applicant
SEIKO OPTICAL PRODUCTS OF AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/1986
Days to Decision
38 days

SEIKO P-2 & SEIKO P-3 (SPECTACLE LENS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861684
510(k) Type
Traditional
Applicant
SEIKO OPTICAL PRODUCTS OF AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/1986
Days to Decision
38 days