PARAGON CZE 2000 CLINICAL CAPILLARY ELECTROPHORESIS SYSTEM— 510(k) K953077
Substantially EquivalentBeckman Instruments, Inc.
FDA 510(k) clearance K953077 for PARAGON CZE 2000 CLINICAL CAPILLARY ELECTROPHORESIS SYSTEM, Substantially Equivalent on 1996-01-05. Applicant: Beckman Instruments, Inc.. Device class: 1.
Clearance details
- Applicant
- Beckman Instruments, Inc.
- Product code
- Code CDF
- Device class
- Class 1
- Regulation
- 21 CFR 862.1795
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Brea, CA, US
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