CYTOSCAN(R) DX— 510(k) DEN130018
UnknownAffymetrix, Inc.
FDA 510(k) clearance DEN130018 for CYTOSCAN(R) DX, Unknown on 2014-01-17. Applicant: Affymetrix, Inc.. Device class: 2.
Clearance details
- Applicant
- Affymetrix, Inc.
- Product code
- Code PFX
- Device class
- Class 2
- Regulation
- 21 CFR 866.5920
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- Santa Clara, CA, US
Recent devices under product code PFX
view allMore clearances from Affymetrix, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.