FDA 510(k)

CDX80

K-Number: K842536 · 1984-08-17

Decision Date1984-08-17

Product CodeBZG

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

CDX80 is the device name listed in this FDA 510(k) record. The listed applicant is Cdx Corp.. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K842536. 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 CDX80?

CDX80 is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Cdx Corp.. The 510(k) number is K842536.

When did CDX80 receive FDA 510(k) clearance?

CDX80 received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842536.

Who is the listed applicant for CDX80?

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 CDX80?

The FDA product code for CDX80 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 K820035CDX 200 K820036CXD 400

Related Devices (Code: BZG)

K251777MESI mTABLET SPIROMesi D.O.O.K241843TD-7301 Spirometer (TD-7301)Gostar Co., Ltd.K231416Air Next (NVD-02)Nuvoair AB K230501Spirobank OxiMir Medical International Research USA K230178EasyOne Sky SpirometerNdd Medizintechnik AG K222525Alveoair Digital SpirometerRoundworks Technologies Private Limited

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.