Last synced on 14 November 2025 at 11:06 pm

ULTRA-WIDE SAFETY SPECTACLE FRAME

Page Type
Cleared 510(K)
510(k) Number
K813156
510(k) Type
Traditional
Applicant
ZEE MEDICAL PRODUCTS CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/1981
Days to Decision
38 days

ULTRA-WIDE SAFETY SPECTACLE FRAME

Page Type
Cleared 510(K)
510(k) Number
K813156
510(k) Type
Traditional
Applicant
ZEE MEDICAL PRODUCTS CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/1981
Days to Decision
38 days