Compex HD— 510(k) K182017
Substantially EquivalentAddent, Inc.
FDA 510(k) clearance K182017 for Compex HD, Substantially Equivalent on 2019-04-29. Applicant: Addent, Inc.. Device class: 1.
Clearance details
- Applicant
- Addent, Inc.
- Product code
- Code QGO
- Device class
- Class 1
- Regulation
- 21 CFR 872.6100
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Danbury, CT, US
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