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PATIENT EXAMINATION GLOVES (NON STERILE)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895657
510(k) Type
Traditional
Applicant
KA HUNG DEVELOPMENT LTD.
Country
Hong Kong SAR China
FDA Decision
Substantially Equivalent
Decision Date
12/11/1989
Days to Decision
82 days

PATIENT EXAMINATION GLOVES (NON STERILE)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895657
510(k) Type
Traditional
Applicant
KA HUNG DEVELOPMENT LTD.
Country
Hong Kong SAR China
FDA Decision
Substantially Equivalent
Decision Date
12/11/1989
Days to Decision
82 days