DRI-CLAVE LIQUID KLEENZALL— 510(k) K880754
Substantially EquivalentColumbus Dental Mfg. Co.
FDA 510(k) clearance K880754 for DRI-CLAVE LIQUID KLEENZALL, Substantially Equivalent on 1988-05-12. Applicant: Columbus Dental Mfg. Co..
Clearance details
- Applicant
- Columbus Dental Mfg. Co.
- Product code
- Code EHZ
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Louis, MO, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.