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SUNMAX ENTERPRISE SHANGHAI CO. POWDER FREE BLUE NITRILE PATIENT EXAMINATION GLOVE TESTED WITH CHEMOTHERAPY DRUGS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090336
510(k) Type
Traditional
Applicant
Sunmax Enterprise Shanghai Co. , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2009
Days to Decision
141 days
Submission Type
Summary

SUNMAX ENTERPRISE SHANGHAI CO. POWDER FREE BLUE NITRILE PATIENT EXAMINATION GLOVE TESTED WITH CHEMOTHERAPY DRUGS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090336
510(k) Type
Traditional
Applicant
Sunmax Enterprise Shanghai Co. , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2009
Days to Decision
141 days
Submission Type
Summary