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POWDERED LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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