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FDA 510(k)

DIGITAL FLUOROGRAPHIC X-RAY SYSTEM

K-Number: K827760 · 1982-08-10

ApplicantGeneral Electric Co.
Decision Date1982-08-10
Product Code
DecisionSubstantially Equivalent

Device Summary

DIGITAL FLUOROGRAPHIC 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 1982-08-10 under 510(k) number K827760. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL FLUOROGRAPHIC X-RAY SYSTEM?

DIGITAL FLUOROGRAPHIC X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 1982-08-10. The listed applicant is General Electric Co.. The 510(k) number is K827760.

When did DIGITAL FLUOROGRAPHIC X-RAY SYSTEM receive FDA 510(k) clearance?

DIGITAL FLUOROGRAPHIC X-RAY SYSTEM received FDA 510(k) clearance on 1982-08-10, under 510(k) number K827760.

Who is the listed applicant for DIGITAL FLUOROGRAPHIC X-RAY SYSTEM?

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

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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 OPTIONK082317GE LUNAR FRAX 10-YEAR FRACTURE RISK SOFTWARE OPTIONK081921GE VIVID E9 ULTRASOUNDK073297GE LOGIQ P6K072952GE ECHOPACK072797GE 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.

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