Last synced on 25 January 2026 at 3:41 am

SYNTEX PRE-POWDERED LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
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
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