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SYNTEX PRE-POWDERED LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022092
510(k) Type
Traditional
Applicant
SYNTEX HEALTHCARE PRODUCTS CO. LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/3/2002
Days to Decision
68 days
Submission Type
Statement

SYNTEX PRE-POWDERED LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022092
510(k) Type
Traditional
Applicant
SYNTEX HEALTHCARE PRODUCTS CO. LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/3/2002
Days to Decision
68 days
Submission Type
Statement