510(k) DEN040010
- Device
- VYSIS AUTOVYSION SYSTEM
- Applicant
- Vysis
- 510(k) number
- DEN040010
- Product code
- NTH
- Decision
- Unknown (DENG)
- Decision date
- 2004-12-13
- Date received
- 2004-10-13
- Regulation
- 866.4700
- Classification name
- System, Automated Scanning Microscope And Image Analysis For Fluorescence In Situ Hybridization (Fish) Assays
- Medical specialty
- Immunology
- Review panel
- Immunology
- Device class
- 2
- Clearance type
- Post-NSE
- Third party reviewed
- N
Applicant Contact#
- Contact
- LYNDA HAGUE
- Address
- 3100 Woodcreek Dr. Downers Grove IL US 60515 60515
FDA Registration Numbers#
- 3003909093
- 3005248192
- 9615060
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code NTH#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K130775 | DUET SYSTEM | Bioview , Ltd. | 2014-05-09 |
| K122554 | GENASIS SCANVIEW SYSTEM | Applied Spectral Imaging , Ltd. | 2013-02-07 |
| K110345 | SCANVIEW SYSTEM | Applied Spectral Imaging | 2011-10-19 |
| K101291 | SCANVIEW HER2/NEU FISH SYSTEM | Applied Spectral Imaging , Ltd. | 2010-11-23 |
| K080909 | ICONOSCOPE ONCOFISH HER2 TEST SYSTEM, MODEL 2000 | Ikonisys, Inc. | 2008-10-17 |
| K043519 | ARIOL HER-2/NEU FISH | Applied Imaging Corp. | 2005-04-25 |
| K042542 | CYTOVISION FOR CEP XY | Applied Imaging Corp. | 2005-01-10 |