ARIOL— 510(k) K033200
Substantially EquivalentApplied Imaging Corp.
FDA 510(k) clearance K033200 for ARIOL, Substantially Equivalent on 2004-03-18. Applicant: Applied Imaging Corp.. Device class: 2.
Clearance details
- Applicant
- Applied Imaging Corp.
- Product code
- Code NQN
- Device class
- Class 2
- Regulation
- 21 CFR 864.1860
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Clara, CA, US
Recent devices under product code NQN
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view allRecalls naming K033200
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K033200.
Data sourced from openFDA. This site is unofficial and independent of the FDA.