OsteoProbe— 510(k) K221195
Substantially EquivalentActive Life Scientific, Inc.
FDA 510(k) clearance K221195 for OsteoProbe, Substantially Equivalent on 2022-06-28. Applicant: Active Life Scientific, Inc.. Device class: 2.
Clearance details
- Applicant
- Active Life Scientific, Inc.
- Product code
- Code QGQ
- Device class
- Class 2
- Regulation
- 21 CFR 888.1600
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Santa Barbara, CA, US
Recent devices under product code QGQ
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