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LATEX PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K895023
510(k) Type
Traditional
Applicant
BEIJING LATEX FACTORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1989
Days to Decision
119 days

LATEX PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K895023
510(k) Type
Traditional
Applicant
BEIJING LATEX FACTORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1989
Days to Decision
119 days