Miha Bodytec II— 510(k) K182519
Substantially EquivalentMiha Bodytec GmbH
FDA 510(k) clearance K182519 for Miha Bodytec II, Substantially Equivalent on 2019-06-07. Applicant: Miha Bodytec GmbH. Device class: 2.
Clearance details
- Applicant
- Miha Bodytec GmbH
- Product code
- Code NGX
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Gersthofen, DE
Recent devices under product code NGX
view allMore clearances from Miha Bodytec GmbH
view allData sourced from openFDA. This site is unofficial and independent of the FDA.