PHENYTOIN REAGENT TEST KIT— 510(k) K802038
Substantially EquivalentBeckman Instruments, Inc.
FDA 510(k) clearance K802038 for PHENYTOIN REAGENT TEST KIT, Substantially Equivalent on 1980-10-23. Applicant: Beckman Instruments, Inc..
Clearance details
- Applicant
- Beckman Instruments, Inc.
- Product code
- Code DID
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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