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LATEXX MANUFACTURING NON-CHLORINATED, POLYMER COATED, POWDER-FREE RUBBER LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014087
510(k) Type
Traditional
Applicant
LATEXX MANUFACTURING SDN.BHD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2002
Days to Decision
83 days
Submission Type
Statement

LATEXX MANUFACTURING NON-CHLORINATED, POLYMER COATED, POWDER-FREE RUBBER LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014087
510(k) Type
Traditional
Applicant
LATEXX MANUFACTURING SDN.BHD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2002
Days to Decision
83 days
Submission Type
Statement