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OMNI GRIP LATEX EXAMINATION GLOVE, POWDER-FREE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964563
510(k) Type
Traditional
Applicant
Omni Sales Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1996
Days to Decision
46 days
Submission Type
Statement

OMNI GRIP LATEX EXAMINATION GLOVE, POWDER-FREE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964563
510(k) Type
Traditional
Applicant
Omni Sales Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1996
Days to Decision
46 days
Submission Type
Statement