CLINITEK 50 URINE CHEMISTRY ANALYZER— 510(k) K960546
Substantially EquivalentBayer Corp.
FDA 510(k) clearance K960546 for CLINITEK 50 URINE CHEMISTRY ANALYZER, Substantially Equivalent on 1996-06-12. Applicant: Bayer Corp.. Device class: 1.
Clearance details
- Applicant
- Bayer Corp.
- Product code
- Code KQO
- Device class
- Class 1
- Regulation
- 21 CFR 862.2900
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Elkhart, IN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.