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PROTEX LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K900790
510(k) Type
Traditional
Applicant
SEYEN INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1990
Days to Decision
44 days

PROTEX LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K900790
510(k) Type
Traditional
Applicant
SEYEN INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1990
Days to Decision
44 days