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OMNI GRACE LATEX EXAMINATION GLOVE, POWDERED, WITH PROTEIN CLAIM (200 MICROGRAMS OR LESS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002922
510(k) Type
Traditional
Applicant
OMNIGRACE (THAILAND) LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2000
Days to Decision
27 days
Submission Type
Statement

OMNI GRACE LATEX EXAMINATION GLOVE, POWDERED, WITH PROTEIN CLAIM (200 MICROGRAMS OR LESS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002922
510(k) Type
Traditional
Applicant
OMNIGRACE (THAILAND) LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2000
Days to Decision
27 days
Submission Type
Statement