CDX 200— 510(k) K820035

Substantially Equivalent

Cdx Corp.

FDA 510(k) clearance K820035 for CDX 200, Substantially Equivalent on 1982-03-10. Applicant: Cdx Corp.. Device class: 2.

Clearance details

Applicant: Cdx Corp.
Product code: Code BZM
Device class: Class 2
Regulation: 21 CFR 868.1900
Advisory panel: Anesthesiology
Date received: 1982-01-07
Decision date: 1982-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BZM

K102229 — PULMOTRACK 2020 SYSTEM2011-03-04
K090863 — PERSONAL WHEEZOMETER2009-09-21
K071955 — WIM-PC, MODEL 10102007-11-01
K012387 — STG MULTICHANNEL LUNG SOUND ANALYSIS SYSTEM2002-04-23
K980878 — PULMOTRACK,MODEL 10101998-12-28

More clearances from Cdx Corp.

Data sourced from openFDA. This site is unofficial and independent of the FDA.