AposTherapy System— 510(k) K182090
Substantially EquivalentApos Medical Assets , Ltd.
FDA 510(k) clearance K182090 for AposTherapy System, Substantially Equivalent on 2018-11-16. Applicant: Apos Medical Assets , Ltd.. Device class: 1.
Clearance details
- Applicant
- Apos Medical Assets , Ltd.
- Product code
- Code QDT
- Device class
- Class 1
- Regulation
- 21 CFR 890.3475
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tel Aviv, IL
Data sourced from openFDA. This site is unofficial and independent of the FDA.