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STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000891
510(k) Type
Traditional
Applicant
FITCO DIPPED PRODUCTS PVT. LTD
Country
India
FDA Decision
Substantially Equivalent
Decision Date
4/28/2000
Days to Decision
39 days
Submission Type
Statement

STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000891
510(k) Type
Traditional
Applicant
FITCO DIPPED PRODUCTS PVT. LTD
Country
India
FDA Decision
Substantially Equivalent
Decision Date
4/28/2000
Days to Decision
39 days
Submission Type
Statement