Last synced on 25 January 2026 at 3:41 am

POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070760
510(k) Type
Traditional
Applicant
Derma Care Plus Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2007
Days to Decision
79 days
Submission Type
Statement

POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070760
510(k) Type
Traditional
Applicant
Derma Care Plus Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2007
Days to Decision
79 days
Submission Type
Statement