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PATIENT EXAMINATION GLOVE, NITRILE, POWDERED, TURQUOISE, NON-STERILE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991846
510(k) Type
Traditional
Applicant
OMNIGRACE LTD.
Country
Thailand
FDA Decision
Substantially Equivalent
Decision Date
8/5/1999
Days to Decision
69 days
Submission Type
Statement

PATIENT EXAMINATION GLOVE, NITRILE, POWDERED, TURQUOISE, NON-STERILE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991846
510(k) Type
Traditional
Applicant
OMNIGRACE LTD.
Country
Thailand
FDA Decision
Substantially Equivalent
Decision Date
8/5/1999
Days to Decision
69 days
Submission Type
Statement