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PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892279
510(k) Type
Traditional
Applicant
AEK RUBBER PRODUCT SDN. BHD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1989
Days to Decision
241 days

PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892279
510(k) Type
Traditional
Applicant
AEK RUBBER PRODUCT SDN. BHD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1989
Days to Decision
241 days