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LATEX POWDERED PATIENT EXAMINATION GLOVE, 200 MICROGRAMS OR LESS

Page Type
Cleared 510(K)
510(k) Number
K011749
510(k) Type
Traditional
Applicant
SEMPERMED USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2001
Days to Decision
83 days
Submission Type
Summary

LATEX POWDERED PATIENT EXAMINATION GLOVE, 200 MICROGRAMS OR LESS

Page Type
Cleared 510(K)
510(k) Number
K011749
510(k) Type
Traditional
Applicant
SEMPERMED USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2001
Days to Decision
83 days
Submission Type
Summary