ACUPRESS VIBRATOR— 510(k) K812902
Substantially EquivalentEicona Corp.
FDA 510(k) clearance K812902 for ACUPRESS VIBRATOR, Substantially Equivalent on 1981-11-10. Applicant: Eicona Corp.. Device class: 1.
Clearance details
- Applicant
- Eicona Corp.
- Product code
- Code IRO
- Device class
- Class 1
- Regulation
- 21 CFR 890.5975
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code IRO
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