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LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K900499
510(k) Type
Traditional
Applicant
PREMIUM FIT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/1990
Days to Decision
34 days

LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K900499
510(k) Type
Traditional
Applicant
PREMIUM FIT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/1990
Days to Decision
34 days