REMEDI(TM) DRUG PROFILING SYSTEM, MODIFICATION— 510(k) K911954
Substantially EquivalentBio-Rad
FDA 510(k) clearance K911954 for REMEDI(TM) DRUG PROFILING SYSTEM, MODIFICATION, Substantially Equivalent on 1991-05-23. Applicant: Bio-Rad. Device class: 2.
Clearance details
- Applicant
- Bio-Rad
- Product code
- Code DJR
- Device class
- Class 2
- Regulation
- 21 CFR 862.3620
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hercules, CA, US
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