X-Ray System for Dental Application

FDA 510(k) K772184 · General Electric Co.

Substantially Equivalent

510(k) numberK772184

Submission

Device name
X-Ray System for Dental Application
Applicant
General Electric Co.
Mchenry, IL, US
Received
November 25, 1977
Decision date
December 22, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EAP – Unit, X-Ray, Intraoral
Device class
Class II (moderate risk)
Regulation
21 CFR 872.1810
Specialty
Dental

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K113360Medical Image Processing UnitEAP · Special Humanray Co,Ltd02/07/2012SE
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K093453Modification to Computed Oral Radiology SystemEAP · Special Schick Technologies, Inc.11/30/2009SE
K080738Dentron SensorEAP · Traditional Dentron Systems, LLC05/13/2008SE
K052422The Envision Intraoral Dental X-Ray Machines (Wall Mounted and Mobile)EAP · Special Flow X-Ray Corp.09/27/2005SE
K041385Modification to Computed Oral Radiology SystemEAP · Special Schick Technologies, Inc.06/07/2004SE
K960819Heliodent DSEAP · Traditional Pelton & Crane Co.03/29/1996SE
K960028Orthoralix SD2 & S Panoramic Dental X-Ray SystemEAP · Traditional Dentsply Intl.03/01/1996SE
K953936AtlantisEAP · Traditional Trophy Radiologie12/28/1995SE
K954565Explor-X (Azteh) HFEAP · Traditional Chicago X-Ray Systems, Inc.10/27/1995SE

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Questions and answers

When was X-Ray System for Dental Application cleared by the FDA?

X-Ray System for Dental Application (K772184) received a 510(k) decision of Substantially Equivalent on December 22, 1977, 27 days after the submission was received.

What is the product code of K772184?

The FDA product code is EAP – Unit, X-Ray, Intraoral, a Class II (moderate risk) device regulated under 21 CFR 872.1810.