ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY— 510(k) K820616
Substantially EquivalentE. R. Squibb & Sons, Inc.
FDA 510(k) clearance K820616 for ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY, Substantially Equivalent on 1982-03-26. Applicant: E. R. Squibb & Sons, Inc.. Device class: 2.
Clearance details
- Applicant
- E. R. Squibb & Sons, Inc.
- 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
- New York, NY, 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 E. R. Squibb & Sons, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.