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PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K891017
510(k) Type
Traditional
Applicant
PARAMOUNT PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1989
Days to Decision
37 days

PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K891017
510(k) Type
Traditional
Applicant
PARAMOUNT PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1989
Days to Decision
37 days