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TEKMEDIC POWDERED SINGLE-USE LATEX PATIENT EXAMINATION GLOVES WITH PROTEIN & POWDER LABEL CLAIM CONTAINS 70MGM OR LESS O

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000555
510(k) Type
Traditional
Applicant
Tekmedic (M) Sdn Bhd
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2000
Days to Decision
54 days
Submission Type
Statement

TEKMEDIC POWDERED SINGLE-USE LATEX PATIENT EXAMINATION GLOVES WITH PROTEIN & POWDER LABEL CLAIM CONTAINS 70MGM OR LESS O

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000555
510(k) Type
Traditional
Applicant
Tekmedic (M) Sdn Bhd
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2000
Days to Decision
54 days
Submission Type
Statement