DAB DETECTION KIT— 510(k) K920600
Substantially EquivalentVentana Medical Systems, Inc.
FDA 510(k) clearance K920600 for DAB DETECTION KIT, Substantially Equivalent on 1992-05-11. Applicant: Ventana Medical Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Ventana Medical Systems, Inc.
- Product code
- Code DEY
- Device class
- Class 2
- Regulation
- 21 CFR 866.5550
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tucson, AZ, US
Recent devices under product code DEY
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