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FDA 510(k)

GENOX MODEL CT-1

K-Number: K904639 · 1991-08-13

Decision Date1991-08-13
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GENOX MODEL CT-1 is the device name listed in this FDA 510(k) record. The listed applicant is Pacific Consolidated Industries. It received FDA 510(k) clearance on 1991-08-13 under 510(k) number K904639. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENOX MODEL CT-1?

GENOX MODEL CT-1 is a medical device that received FDA 510(k) clearance on 1991-08-13. The listed applicant is Pacific Consolidated Industries. The 510(k) number is K904639.

When did GENOX MODEL CT-1 receive FDA 510(k) clearance?

GENOX MODEL CT-1 received FDA 510(k) clearance on 1991-08-13, under 510(k) number K904639.

Who is the listed applicant for GENOX MODEL CT-1?

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

What is the FDA product code for GENOX MODEL CT-1?

The FDA product code for GENOX MODEL CT-1 is CAW.

Related Clinical Trials

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.

Other records listing Pacific Consolidated Industries 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.

Related Devices (Code: CAW)

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.

Official Source

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