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OMNI PRO LATEX SURGICAL GLOVE, POWDERED

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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