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LATEX EXAMINATION GLOVE (POWDERED)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014280
510(k) Type
Traditional
Applicant
BRIGHTWAY GLOVES PVT. LTD.
Country
India
FDA Decision
Substantially Equivalent
Decision Date
3/20/2002
Days to Decision
83 days
Submission Type
Summary

LATEX EXAMINATION GLOVE (POWDERED)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014280
510(k) Type
Traditional
Applicant
BRIGHTWAY GLOVES PVT. LTD.
Country
India
FDA Decision
Substantially Equivalent
Decision Date
3/20/2002
Days to Decision
83 days
Submission Type
Summary