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FDA 510(k)

X-RAY SYSTEM FOR DENTAL APPLICATION

K-Number: K772184 · 1977-12-22

Decision Date1977-12-22
Product CodeEAP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

X-RAY SYSTEM FOR DENTAL APPLICATION 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 1977-12-22 under 510(k) number K772184. 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 X-RAY SYSTEM FOR DENTAL APPLICATION?

X-RAY SYSTEM FOR DENTAL APPLICATION is a medical device that received FDA 510(k) clearance on 1977-12-22. The listed applicant is General Electric Co.. The 510(k) number is K772184.

When did X-RAY SYSTEM FOR DENTAL APPLICATION receive FDA 510(k) clearance?

X-RAY SYSTEM FOR DENTAL APPLICATION received FDA 510(k) clearance on 1977-12-22, under 510(k) number K772184.

Who is the listed applicant for X-RAY SYSTEM FOR DENTAL APPLICATION?

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 X-RAY SYSTEM FOR DENTAL APPLICATION?

The FDA product code for X-RAY SYSTEM FOR DENTAL APPLICATION is EAP.

Related Clinical Trials

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.

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.

View all 254 devices →

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.

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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