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PATIENT EXAMINATION GLOVE (LATEX)

Page Type
Cleared 510(K)
510(k) Number
K891271
510(k) Type
Traditional
Applicant
DR. BOO CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1989
Days to Decision
13 days

PATIENT EXAMINATION GLOVE (LATEX)

Page Type
Cleared 510(K)
510(k) Number
K891271
510(k) Type
Traditional
Applicant
DR. BOO CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1989
Days to Decision
13 days