HYDROFLEX— 510(k) K973343
Substantially EquivalentGC America, Inc.
FDA 510(k) clearance K973343 for HYDROFLEX, Substantially Equivalent on 1997-10-21. Applicant: GC America, Inc..
Clearance details
- Applicant
- GC America, Inc.
- Product code
- Code ELW
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Alsip, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.