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LATEX PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K895497
510(k) Type
Traditional
Applicant
PLYMOUTH LTD.
Country
Hong Kong SAR China
FDA Decision
Substantially Equivalent
Decision Date
11/21/1989
Days to Decision
85 days

LATEX PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K895497
510(k) Type
Traditional
Applicant
PLYMOUTH LTD.
Country
Hong Kong SAR China
FDA Decision
Substantially Equivalent
Decision Date
11/21/1989
Days to Decision
85 days