ASPRI-LUKE— 510(k) K791847
Substantially EquivalentMedical Marketing Group
FDA 510(k) clearance K791847 for ASPRI-LUKE, Substantially Equivalent on 1979-10-02. Applicant: Medical Marketing Group. Device class: 2.
Clearance details
- Applicant
- Medical Marketing Group
- Product code
- Code BYZ
- Device class
- Class 2
- Regulation
- 21 CFR 880.6740
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Decatur, GA, US
Recent devices under product code BYZ
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