ANGIOTENSIN CONVERTING ENZYME— 510(k) K833777
Substantially EquivalentImmuno-Diagnostic Laboratories
FDA 510(k) clearance K833777 for ANGIOTENSIN CONVERTING ENZYME, Substantially Equivalent on 1984-01-30. Applicant: Immuno-Diagnostic Laboratories. Device class: 2.
Clearance details
- Applicant
- Immuno-Diagnostic Laboratories
- Product code
- Code CIB
- Device class
- Class 2
- Regulation
- 21 CFR 862.1085
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code CIB
view all- K123763 — IDS ISYS DIRECT RENIN ASSAY, IDS ISYS DIRECT RENIN CONTROL SET, AND IDS ISYS DIRECT RENIN CALIBRATION VERIFIERS
- K121944 — LIAISON DIRECT RENIN LIAISON CONTROL DIRECT RENIN LIAISON ENDOCRINOLOGY DILUENT
- K062120 — CISBIO RENIN RIA TEST
- K061758 — ACTIVE RENIN IRMA
- K011128 — NICHOLS ADVANTAGE DIRECT RENIN (CALIBRATORS, CALIBRATION VERIFIERS, CONTROLS, AND SAMPLE DILUENT)
More clearances from Immuno-Diagnostic Laboratories
view allData sourced from openFDA. This site is unofficial and independent of the FDA.