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OMNI PRO LATEX SURGICAL GLOVE, POWDERED

Page Type
Cleared 510(K)
510(k) Number
K982613
510(k) Type
Traditional
Applicant
OMNIGRACE (THAILAND) LTD.
Country
Thailand
FDA Decision
Substantially Equivalent
Decision Date
9/2/1998
Days to Decision
37 days
Submission Type
Statement

OMNI PRO LATEX SURGICAL GLOVE, POWDERED

Page Type
Cleared 510(K)
510(k) Number
K982613
510(k) Type
Traditional
Applicant
OMNIGRACE (THAILAND) LTD.
Country
Thailand
FDA Decision
Substantially Equivalent
Decision Date
9/2/1998
Days to Decision
37 days
Submission Type
Statement