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PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890931
510(k) Type
Traditional
Applicant
PHUTEX PRODUCTS CO., LTD.
Country
Indonesia
FDA Decision
Substantially Equivalent
Decision Date
6/23/1989
Days to Decision
119 days

PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890931
510(k) Type
Traditional
Applicant
PHUTEX PRODUCTS CO., LTD.
Country
Indonesia
FDA Decision
Substantially Equivalent
Decision Date
6/23/1989
Days to Decision
119 days