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LATEX EXAMINATION GLOVE,POWEDERED TYPE II, LOW MODULUS,WITH PROTEIN LABLING CLAIM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030333
510(k) Type
Traditional
Applicant
Perusahaan Getah Asas Sdn. Bhd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2003
Days to Decision
49 days
Submission Type
Statement

LATEX EXAMINATION GLOVE,POWEDERED TYPE II, LOW MODULUS,WITH PROTEIN LABLING CLAIM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030333
510(k) Type
Traditional
Applicant
Perusahaan Getah Asas Sdn. Bhd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2003
Days to Decision
49 days
Submission Type
Statement