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LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K911081
510(k) Type
Traditional
Applicant
MEDICAL DEVICE INSPECTION CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1991
Days to Decision
10 days

LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K911081
510(k) Type
Traditional
Applicant
MEDICAL DEVICE INSPECTION CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1991
Days to Decision
10 days