CUTTER/COMPUR MINI CENTRIFUGE— 510(k) K781059
Substantially EquivalentCutter Laboratories, Inc.
FDA 510(k) clearance K781059 for CUTTER/COMPUR MINI CENTRIFUGE, Substantially Equivalent on 1978-08-14. Applicant: Cutter Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Cutter Laboratories, Inc.
- Product code
- Code GKF
- Device class
- Class 2
- Regulation
- 21 CFR 864.5600
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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