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POWDERED LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K051913
510(k) Type
Traditional
Applicant
SHINEMOUND ENTERPRISE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2005
Days to Decision
77 days
Submission Type
Statement

POWDERED LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K051913
510(k) Type
Traditional
Applicant
SHINEMOUND ENTERPRISE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2005
Days to Decision
77 days
Submission Type
Statement