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POWDER FREE LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K960467
510(k) Type
Traditional
Applicant
BIOPRO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/1996
Days to Decision
115 days
Submission Type
Statement

POWDER FREE LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K960467
510(k) Type
Traditional
Applicant
BIOPRO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/1996
Days to Decision
115 days
Submission Type
Statement