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OMNIGRIP, LATEX SURGICAL GLOVE, POWDER FREE

Page Type
Cleared 510(K)
510(k) Number
K984064
510(k) Type
Traditional
Applicant
OMNI INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/1999
Days to Decision
53 days
Submission Type
Statement

OMNIGRIP, LATEX SURGICAL GLOVE, POWDER FREE

Page Type
Cleared 510(K)
510(k) Number
K984064
510(k) Type
Traditional
Applicant
OMNI INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/1999
Days to Decision
53 days
Submission Type
Statement