Last synced on 14 November 2025 at 11:06 pm

LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K892573
510(k) Type
Traditional
Applicant
ENCORE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1989
Days to Decision
95 days

LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K892573
510(k) Type
Traditional
Applicant
ENCORE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1989
Days to Decision
95 days