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FDA 510(k)

SR-130

K-Number: K030494 · 2003-05-20

ApplicantSource-Ray, Inc.
Decision Date2003-05-20
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SR-130 is the device name listed in this FDA 510(k) record. The listed applicant is Source-Ray, Inc.. It received FDA 510(k) clearance on 2003-05-20 under 510(k) number K030494. 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 SR-130?

SR-130 is a medical device that received FDA 510(k) clearance on 2003-05-20. The listed applicant is Source-Ray, Inc.. The 510(k) number is K030494.

When did SR-130 receive FDA 510(k) clearance?

SR-130 received FDA 510(k) clearance on 2003-05-20, under 510(k) number K030494.

Who is the listed applicant for SR-130?

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

What is the FDA product code for SR-130?

The FDA product code for SR-130 is IZL.

Other records listing Source-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.

K163063UC-5000 Mobile X-RayK090655PORTABLE X-RAY SYSTEM, MODEL POWERMAX 1260K071392PXS-810, PODIATRY X-RAY SYSTEMK062472OPTIONAL REMOTE CONTROL, MODEL RC-115, FOR PORTABLE X-RAY SYSTEM, MODEL SR-115K052001MODEL SR-115 PORTABLE X-RAY SYSTEMK043062MODEL SR-130-D PORTABLE DIGITAL X-RAY SYSTEM

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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.

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