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LOW POWDER SINGLE USE LATEX EXAM GLOVES

Page Type
Cleared 510(K)
510(k) Number
K892975
510(k) Type
Traditional
Applicant
PHOENIX MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/1989
Days to Decision
68 days

LOW POWDER SINGLE USE LATEX EXAM GLOVES

Page Type
Cleared 510(K)
510(k) Number
K892975
510(k) Type
Traditional
Applicant
PHOENIX MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/1989
Days to Decision
68 days