GENERATOR, R-WAVE— 510(k) K790213
Substantially EquivalentAmr Co.
FDA 510(k) clearance K790213 for GENERATOR, R-WAVE, Substantially Equivalent on 1979-03-22. Applicant: Amr Co.. Device class: 1.
Clearance details
- Applicant
- Amr Co.
- Product code
- Code IYY
- Device class
- Class 1
- Regulation
- 21 CFR 892.1410
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code IYY
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