APEX ELECTRIC HANDPIECE SYSTEM— 510(k) K031540
Substantially EquivalentLares Research, Inc.
FDA 510(k) clearance K031540 for APEX ELECTRIC HANDPIECE SYSTEM, Substantially Equivalent on 2003-06-30. Applicant: Lares Research, Inc.. Device class: 1.
Clearance details
- Applicant
- Lares Research, Inc.
- Product code
- Code EKX
- Device class
- Class 1
- Regulation
- 21 CFR 872.4200
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chico, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.