FDA 510(k)

CDX 200

K-Number: K820035 · 1982-03-10

Decision Date1982-03-10

Product CodeBZM

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

CDX 200 is the device name listed in this FDA 510(k) record. The listed applicant is Cdx Corp.. It received FDA 510(k) clearance on 1982-03-10 under 510(k) number K820035. The device is classified under product code BZM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CDX 200?

CDX 200 is a medical device that received FDA 510(k) clearance on 1982-03-10. The listed applicant is Cdx Corp.. The 510(k) number is K820035.

When did CDX 200 receive FDA 510(k) clearance?

CDX 200 received FDA 510(k) clearance on 1982-03-10, under 510(k) number K820035.

Who is the listed applicant for CDX 200?

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 CDX 200?

The FDA product code for CDX 200 is BZM.

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 K820036CXD 400

Related Devices (Code: BZM)

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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.