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POWER-FREE NITRILE PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121526
510(k) Type
Traditional
Applicant
Shandong Junchi Medical Products Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2012
Days to Decision
72 days
Submission Type
Summary

POWER-FREE NITRILE PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121526
510(k) Type
Traditional
Applicant
Shandong Junchi Medical Products Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2012
Days to Decision
72 days
Submission Type
Summary