ANTICONVULSANTS III CALIBRATOR KIT— 510(k) K780733
Substantially EquivalentVitek Systems, Inc.
FDA 510(k) clearance K780733 for ANTICONVULSANTS III CALIBRATOR KIT, Substantially Equivalent on 1978-06-22. Applicant: Vitek Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Vitek Systems, Inc.
- Product code
- Code DKH
- Device class
- Class 2
- Regulation
- 21 CFR 862.3350
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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