FDA 510(k)

CORT-EX

K-Number: K926133 · 1993-06-08

Decision Date1993-06-08

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CORT-EX is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1993-06-08 under 510(k) number K926133. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORT-EX?

CORT-EX is a medical device that received FDA 510(k) clearance on 1993-06-08. The listed applicant is General Electric Co.. The 510(k) number is K926133.

When did CORT-EX receive FDA 510(k) clearance?

CORT-EX received FDA 510(k) clearance on 1993-06-08, under 510(k) number K926133.

Who is the listed applicant for CORT-EX?

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

What is the FDA product code for CORT-EX?

The FDA product code for CORT-EX is KPS.

Other records listing General Electric Co. 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.

K103489GE VEO RECONSTRUCTION OPTION K082317GE LUNAR FRAX 10-YEAR FRACTURE RISK SOFTWARE OPTION K081921GE VIVID E9 ULTRASOUND K073297GE LOGIQ P6 K072952GE ECHOPAC K072797GE LOGIQ I COMAPACT ULTRASOUND, GE LOGIQ E COMPACT ULTRASOUND, GE VIVID E COMPACT ULTRASOUND

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Official Source

View on FDA Database →

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