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FDA 510(k)

IMAGE INTENSIFIED FLUOROSCOPIC X-RAY SYSTEM

K-Number: K903196 · 1990-08-10

ApplicantGeneral Electric Co.
Decision Date1990-08-10
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMAGE INTENSIFIED FLUOROSCOPIC X-RAY SYSTEM 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 1990-08-10 under 510(k) number K903196. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMAGE INTENSIFIED FLUOROSCOPIC X-RAY SYSTEM?

IMAGE INTENSIFIED FLUOROSCOPIC X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 1990-08-10. The listed applicant is General Electric Co.. The 510(k) number is K903196.

When did IMAGE INTENSIFIED FLUOROSCOPIC X-RAY SYSTEM receive FDA 510(k) clearance?

IMAGE INTENSIFIED FLUOROSCOPIC X-RAY SYSTEM received FDA 510(k) clearance on 1990-08-10, under 510(k) number K903196.

Who is the listed applicant for IMAGE INTENSIFIED FLUOROSCOPIC X-RAY SYSTEM?

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 IMAGE INTENSIFIED FLUOROSCOPIC X-RAY SYSTEM?

The FDA product code for IMAGE INTENSIFIED FLUOROSCOPIC X-RAY SYSTEM is LLZ.

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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.

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