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POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K070760
510(k) Type
Traditional
Applicant
DERMA CARE PLUS PRODUCTS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2007
Days to Decision
79 days
Submission Type
Statement

POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K070760
510(k) Type
Traditional
Applicant
DERMA CARE PLUS PRODUCTS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2007
Days to Decision
79 days
Submission Type
Statement