Televere Podiatry Digital Imaging System— 510(k) K172124
Substantially EquivalentTelevere Systems
FDA 510(k) clearance K172124 for Televere Podiatry Digital Imaging System, Substantially Equivalent on 2017-11-09. Applicant: Televere Systems. Device class: 2.
Clearance details
- Applicant
- Televere Systems
- Product code
- Code MQB
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Arnold, MD, US
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