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FDA 510(k)

SEDECAL MOBILE DIGITAL DIAGNOSTIC X-RAY

K-Number: K101517 · 2011-08-05

ApplicantSedecal., Sa.
Decision Date2011-08-05
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SEDECAL MOBILE DIGITAL DIAGNOSTIC X-RAY is the device name listed in this FDA 510(k) record. The listed applicant is Sedecal., Sa.. It received FDA 510(k) clearance on 2011-08-05 under 510(k) number K101517. 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 SEDECAL MOBILE DIGITAL DIAGNOSTIC X-RAY?

SEDECAL MOBILE DIGITAL DIAGNOSTIC X-RAY is a medical device that received FDA 510(k) clearance on 2011-08-05. The listed applicant is Sedecal., Sa.. The 510(k) number is K101517.

When did SEDECAL MOBILE DIGITAL DIAGNOSTIC X-RAY receive FDA 510(k) clearance?

SEDECAL MOBILE DIGITAL DIAGNOSTIC X-RAY received FDA 510(k) clearance on 2011-08-05, under 510(k) number K101517.

Who is the listed applicant for SEDECAL MOBILE DIGITAL DIAGNOSTIC X-RAY?

The FDA 510(k) record lists Sedecal., Sa. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEDECAL MOBILE DIGITAL DIAGNOSTIC X-RAY?

The FDA product code for SEDECAL MOBILE DIGITAL DIAGNOSTIC X-RAY is IZL.

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Other records listing Sedecal., Sa. as applicant

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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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