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FDA 510(k)

FLUORICON L300 IMAGE INTENSIFIER

K-Number: K812775 · 1981-11-06

ApplicantGeneral Electric Co.
Decision Date1981-11-06
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FLUORICON L300 IMAGE INTENSIFIER 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 1981-11-06 under 510(k) number K812775. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUORICON L300 IMAGE INTENSIFIER?

FLUORICON L300 IMAGE INTENSIFIER is a medical device that received FDA 510(k) clearance on 1981-11-06. The listed applicant is General Electric Co.. The 510(k) number is K812775.

When did FLUORICON L300 IMAGE INTENSIFIER receive FDA 510(k) clearance?

FLUORICON L300 IMAGE INTENSIFIER received FDA 510(k) clearance on 1981-11-06, under 510(k) number K812775.

Who is the listed applicant for FLUORICON L300 IMAGE INTENSIFIER?

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 FLUORICON L300 IMAGE INTENSIFIER?

The FDA product code for FLUORICON L300 IMAGE INTENSIFIER is JAA.

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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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