Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

X-RAY UNIT, PORTABLE GX-101 AEC

K-Number: K781030 · 1978-07-17

ApplicantGeneral X-Ray, Inc.
Decision Date1978-07-17
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-RAY UNIT, PORTABLE GX-101 AEC is the device name listed in this FDA 510(k) record. The listed applicant is General X-Ray, Inc.. It received FDA 510(k) clearance on 1978-07-17 under 510(k) number K781030. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-RAY UNIT, PORTABLE GX-101 AEC?

X-RAY UNIT, PORTABLE GX-101 AEC is a medical device that received FDA 510(k) clearance on 1978-07-17. The listed applicant is General X-Ray, Inc.. The 510(k) number is K781030.

When did X-RAY UNIT, PORTABLE GX-101 AEC receive FDA 510(k) clearance?

X-RAY UNIT, PORTABLE GX-101 AEC received FDA 510(k) clearance on 1978-07-17, under 510(k) number K781030.

Who is the listed applicant for X-RAY UNIT, PORTABLE GX-101 AEC?

The FDA 510(k) record lists General X-Ray, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for X-RAY UNIT, PORTABLE GX-101 AEC?

The FDA product code for X-RAY UNIT, PORTABLE GX-101 AEC is IZL.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing General X-Ray, Inc. 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.

K800998ATLAS-S X-RAY SYSTEM W/KETROMAT GEN.K790451X-RAY UNITS, GX-101, UCIS-510 AND GX-111K790392510 CARBINETTE X-RAY UNITK790393PORTABLE X-RAY UNIT, MATRIX S GX-101K790443PORTABLE X-RAY UNITK790511MOBILE X-RAY UNIT

View all 14 devices →

Related Devices (Code: IZL)

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.

K260236XLITEGEMSS HEALTHCARE CO., LTD.K253058Portable DR Imaging SystemShantou Institute of Ultrasonic Instruments Co., Ltd.K260085RAYMO Mobile X-ray System (Model: RAYMO)DRGEM CorporationK253185Lux HD Detectors, DRX-LC Detector, DRX-Revolution Mobile X-Ray SystemCarestream HealthK253244AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini)Poskom Co., Ltd.K250976Airbile-100Poskom Co., Ltd.

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.

↑