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FDA 510(k)

GE-700 INTRA ORAL X-RAY SYSTEM

K-Number: K781630 · 1978-12-04

ApplicantGeneral Electric Co.
Decision Date1978-12-04
Product CodeEAP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GE-700 INTRA ORAL 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 1978-12-04 under 510(k) number K781630. The device is classified under product code EAP. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GE-700 INTRA ORAL X-RAY SYSTEM?

GE-700 INTRA ORAL X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is General Electric Co.. The 510(k) number is K781630.

When did GE-700 INTRA ORAL X-RAY SYSTEM receive FDA 510(k) clearance?

GE-700 INTRA ORAL X-RAY SYSTEM received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781630.

Who is the listed applicant for GE-700 INTRA ORAL 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 GE-700 INTRA ORAL X-RAY SYSTEM?

The FDA product code for GE-700 INTRA ORAL X-RAY SYSTEM is EAP.

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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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Related Devices (Code: EAP)

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.

K113360MEDICAL IMAGE PROCESSING UNITHumanray Co,LtdK102573PROVU (TM) DENTAL X-RAY SYSTEMAdvanced Image Science, Inc.K093453MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEMSchick Technologies, Inc.K080738DENTRON SENSORDentron Systems, LLCK052422THE ENVISION INTRAORAL DENTAL X-RAY MACHINES (WALL MOUNTED AND MOBILE)Flow X-Ray Corp.K041385MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEMSchick Technologies, Inc.

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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