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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
FDA Hosted 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
FDA Hosted 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