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BRIGHTWAY BRAND LATEX EXAMINATION GLOVE-(POWDER FREE, STERILE) CONTAINING 50 UGM OR LESS OF WATER EXTRACTABLE PROTEIN PE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032940
510(k) Type
Traditional
Applicant
Brightway Holdings Sdn. Bhd.
Country
Malaysia
FDA Decision
Substantially Equivalent
Decision Date
11/20/2003
Days to Decision
59 days
Submission Type
Statement

BRIGHTWAY BRAND LATEX EXAMINATION GLOVE-(POWDER FREE, STERILE) CONTAINING 50 UGM OR LESS OF WATER EXTRACTABLE PROTEIN PE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032940
510(k) Type
Traditional
Applicant
Brightway Holdings Sdn. Bhd.
Country
Malaysia
FDA Decision
Substantially Equivalent
Decision Date
11/20/2003
Days to Decision
59 days
Submission Type
Statement