CREATININE (ENZYMATIC UV) PROCEDURE FOR TECHNICON SYSTEMS (IN VITRO DIAGNOSTIC TEST SYSTEM)— 510(k) K945655
Substantially EquivalentMiles, Inc.
FDA 510(k) clearance K945655 for CREATININE (ENZYMATIC UV) PROCEDURE FOR TECHNICON SYSTEMS (IN VITRO DIAGNOSTIC TEST SYSTEM), Substantially Equivalent on 1995-01-05. Applicant: Miles, Inc.. Device class: 2.
Clearance details
- Applicant
- Miles, Inc.
- Product code
- Code CGX
- Device class
- Class 2
- Regulation
- 21 CFR 862.1225
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tarrytown, NY, US
Recent devices under product code CGX
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Data sourced from openFDA. This site is unofficial and independent of the FDA.