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SYNTEX POWDER-FREE NITRILE EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020493
510(k) Type
Traditional
Applicant
SYNTEX HEALTHCARE PRODUCTS CO. LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/26/2002
Days to Decision
13 days
Submission Type
Statement

SYNTEX POWDER-FREE NITRILE EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020493
510(k) Type
Traditional
Applicant
SYNTEX HEALTHCARE PRODUCTS CO. LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/26/2002
Days to Decision
13 days
Submission Type
Statement