RANDOX PHENCYCLIDINE ASSAY— 510(k) K043071
Substantially EquivalentRandox Laboratories, Ltd.
FDA 510(k) clearance K043071 for RANDOX PHENCYCLIDINE ASSAY, Substantially Equivalent on 2005-01-27. Applicant: Randox Laboratories, Ltd.. Device class: Unclassified.
Clearance details
- Applicant
- Randox Laboratories, Ltd.
- Product code
- Code LCM
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Crumlin, GB
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