FDA 510(k)

CXD 400

K-Number: K820036 · 1982-01-22

Decision Date1982-01-22

Product CodeBZG

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

CXD 400 is the device name listed in this FDA 510(k) record. The listed applicant is Cdx Corp.. It received FDA 510(k) clearance on 1982-01-22 under 510(k) number K820036. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CXD 400?

CXD 400 is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Cdx Corp.. The 510(k) number is K820036.

When did CXD 400 receive FDA 510(k) clearance?

CXD 400 received FDA 510(k) clearance on 1982-01-22, under 510(k) number K820036.

Who is the listed applicant for CXD 400?

The FDA 510(k) record lists Cdx Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CXD 400?

The FDA product code for CXD 400 is BZG.

Other records listing Cdx Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K853190SUPERSPIRO K842536CDX80 K820035CDX 200

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.