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PATIENT LATEX EXAMINATION GLOVE (PREPOWDERED)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971629
510(k) Type
Traditional
Applicant
BESGLOVE MEDICARE SDN. BHD.
Country
Malaysia
FDA Decision
Substantially Equivalent
Decision Date
8/6/1997
Days to Decision
96 days
Submission Type
Statement

PATIENT LATEX EXAMINATION GLOVE (PREPOWDERED)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971629
510(k) Type
Traditional
Applicant
BESGLOVE MEDICARE SDN. BHD.
Country
Malaysia
FDA Decision
Substantially Equivalent
Decision Date
8/6/1997
Days to Decision
96 days
Submission Type
Statement