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PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K891972
510(k) Type
Traditional
Applicant
GRANDTECH RUBBER PRODUCTS CO. LTD.
Country
Hong Kong SAR China
FDA Decision
Substantially Equivalent
Decision Date
5/12/1989
Days to Decision
44 days

PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K891972
510(k) Type
Traditional
Applicant
GRANDTECH RUBBER PRODUCTS CO. LTD.
Country
Hong Kong SAR China
FDA Decision
Substantially Equivalent
Decision Date
5/12/1989
Days to Decision
44 days