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MODIFIED SINGLE USE LATEX EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K900453
510(k) Type
Traditional
Applicant
PHOENIX MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1990
Days to Decision
14 days

MODIFIED SINGLE USE LATEX EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K900453
510(k) Type
Traditional
Applicant
PHOENIX MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1990
Days to Decision
14 days