Last synced on 14 November 2025 at 11:06 pm

SEMPERMED LATEX EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K896428
510(k) Type
Traditional
Applicant
SEMPERIT INDUSTRIAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1990
Days to Decision
65 days

SEMPERMED LATEX EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K896428
510(k) Type
Traditional
Applicant
SEMPERIT INDUSTRIAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1990
Days to Decision
65 days