IN VITRO TEST DETERMINATION OF INORGANIC PHOSPHORO— 510(k) K854188
Substantially EquivalentClinical Data, Inc.
FDA 510(k) clearance K854188 for IN VITRO TEST DETERMINATION OF INORGANIC PHOSPHORO, Substantially Equivalent on 1985-11-25. Applicant: Clinical Data, Inc.. Device class: 1.
Clearance details
- Applicant
- Clinical Data, Inc.
- Product code
- Code CEO
- Device class
- Class 1
- Regulation
- 21 CFR 862.1580
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Boston, MA, US
Recent devices under product code CEO
view allMore clearances from Clinical Data, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.