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NON-STERILE, POWDERED LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K081910
510(k) Type
Abbreviated
Applicant
SIAM SEMPERMED CORP. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2008
Days to Decision
76 days
Submission Type
Summary

NON-STERILE, POWDERED LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K081910
510(k) Type
Abbreviated
Applicant
SIAM SEMPERMED CORP. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2008
Days to Decision
76 days
Submission Type
Summary