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PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
510(k) Number
K892567
510(k) Type
Traditional
Applicant
ANHUI LIGHT INDUSTRIAL PRODUCTS I/E CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1989
Days to Decision
45 days

PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
510(k) Number
K892567
510(k) Type
Traditional
Applicant
ANHUI LIGHT INDUSTRIAL PRODUCTS I/E CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1989
Days to Decision
45 days