CLINIC 2000 MODEL MULTI-FRECODYN DEVICE— 510(k) K820784
Substantially EquivalentDimeco
FDA 510(k) clearance K820784 for CLINIC 2000 MODEL MULTI-FRECODYN DEVICE, Substantially Equivalent on 1982-04-22. Applicant: Dimeco. Device class: 2.
Clearance details
- Applicant
- Dimeco
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code IPF
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