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DIGIFLEX, LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K910542
510(k) Type
Traditional
Applicant
21ST CENTURY GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1991
Days to Decision
14 days

DIGIFLEX, LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K910542
510(k) Type
Traditional
Applicant
21ST CENTURY GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1991
Days to Decision
14 days