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OMNI F.T. LATEX EXAMINATION GLOVE, POWDERED

Page Type
Cleared 510(K)
510(k) Number
K973134
510(k) Type
Traditional
Applicant
OMNIGRACE LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1997
Days to Decision
77 days
Submission Type
Statement

OMNI F.T. LATEX EXAMINATION GLOVE, POWDERED

Page Type
Cleared 510(K)
510(k) Number
K973134
510(k) Type
Traditional
Applicant
OMNIGRACE LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1997
Days to Decision
77 days
Submission Type
Statement