PRIMIDONE (FPIA) KIT— 510(k) K895567
Substantially EquivalentTudor Laboratories, Inc.
FDA 510(k) clearance K895567 for PRIMIDONE (FPIA) KIT, Substantially Equivalent on 1989-10-20. Applicant: Tudor Laboratories, Inc..
Clearance details
- Applicant
- Tudor Laboratories, Inc.
- Product code
- Code LFT
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dallas, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.