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DR. BOO LATEX EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K893520
510(k) Type
Traditional
Applicant
DYNATECH MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1989
Days to Decision
105 days

DR. BOO LATEX EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K893520
510(k) Type
Traditional
Applicant
DYNATECH MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1989
Days to Decision
105 days