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PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K892974
510(k) Type
Traditional
Applicant
DUBO LATEX LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1989
Days to Decision
127 days

PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K892974
510(k) Type
Traditional
Applicant
DUBO LATEX LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1989
Days to Decision
127 days