CONVERTRAY, MODIFICATION— 510(k) K912001
Substantially EquivalentWilde Dental (Usa)
FDA 510(k) clearance K912001 for CONVERTRAY, MODIFICATION, Substantially Equivalent on 1992-01-09. Applicant: Wilde Dental (Usa). Device class: 2.
Clearance details
- Applicant
- Wilde Dental (Usa)
- Product code
- Code ELW
- Device class
- Class 2
- Regulation
- 21 CFR 872.3660
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chicago, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.