Last synced on 14 November 2025 at 11:06 pm

AQUALUX LENS CASE

Page Type
Cleared 510(K)
510(k) Number
K862811
510(k) Type
Traditional
Applicant
SAFEWAY PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/1986
Days to Decision
41 days

AQUALUX LENS CASE

Page Type
Cleared 510(K)
510(k) Number
K862811
510(k) Type
Traditional
Applicant
SAFEWAY PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/1986
Days to Decision
41 days