BIOTRACK PHENYTOIN TEST CARTRIDGE— 510(k) K915755
Substantially EquivalentBiotrack, Inc.
FDA 510(k) clearance K915755 for BIOTRACK PHENYTOIN TEST CARTRIDGE, Substantially Equivalent on 1992-07-23. Applicant: Biotrack, Inc.. Device class: 2.
Clearance details
- Applicant
- Biotrack, Inc.
- Product code
- Code DIP
- Device class
- Class 2
- Regulation
- 21 CFR 862.3350
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mountain View, CA, US
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More clearances from Biotrack, Inc.
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