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LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895754
510(k) Type
Traditional
Applicant
FRONTLINE LATEX PRODUCTS PVT. LTD.
Country
India
FDA Decision
Substantially Equivalent
Decision Date
12/21/1989
Days to Decision
84 days

LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895754
510(k) Type
Traditional
Applicant
FRONTLINE LATEX PRODUCTS PVT. LTD.
Country
India
FDA Decision
Substantially Equivalent
Decision Date
12/21/1989
Days to Decision
84 days