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OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIM

Page Type
Cleared 510(K)
510(k) Number
K984066
510(k) Type
Traditional
Applicant
OMNI INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/1999
Days to Decision
58 days
Submission Type
Statement

OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIM

Page Type
Cleared 510(K)
510(k) Number
K984066
510(k) Type
Traditional
Applicant
OMNI INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/1999
Days to Decision
58 days
Submission Type
Statement