MULTI-CENTRIFUGE— 510(k) K955795
Substantially EquivalentNovonx, Inc.
FDA 510(k) clearance K955795 for MULTI-CENTRIFUGE, Substantially Equivalent on 1996-03-29. Applicant: Novonx, Inc.. Device class: 2.
Clearance details
- Applicant
- Novonx, Inc.
- Product code
- Code GKG
- Device class
- Class 2
- Regulation
- 21 CFR 864.6400
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
Recent devices under product code GKG
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