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PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
510(k) Number
K891975
510(k) Type
Traditional
Applicant
EVER SURPLUS (USA), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/1989
Days to Decision
44 days

PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
510(k) Number
K891975
510(k) Type
Traditional
Applicant
EVER SURPLUS (USA), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/1989
Days to Decision
44 days