Last synced on 23 September 2022 at 11:05 pm

AURALITE II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852403
510(k) Type
Traditional
Applicant
AURA LENS PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1985
Days to Decision
75 days

AURALITE II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852403
510(k) Type
Traditional
Applicant
AURA LENS PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1985
Days to Decision
75 days