CLK INT'L POWDER FREE LATEX EXAMINATION GLOVE— 510(k) K974371
Substantially EquivalentClk Intl., Inc.
FDA 510(k) clearance K974371 for CLK INT'L POWDER FREE LATEX EXAMINATION GLOVE, Substantially Equivalent on 1998-04-21. Applicant: Clk Intl., Inc..
Clearance details
- Applicant
- Clk Intl., Inc.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.