Last synced on 14 November 2025 at 11:06 pm

PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
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)
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