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FDA 510(k)

X-RAY FRAME HOLDER

K-Number: K780999 · 1978-06-27

ApplicantGreat Eastern Lumber Co., Inc.
Decision Date1978-06-27
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-RAY FRAME HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Great Eastern Lumber Co., Inc.. It received FDA 510(k) clearance on 1978-06-27 under 510(k) number K780999. 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 FRAME HOLDER?

X-RAY FRAME HOLDER is a medical device that received FDA 510(k) clearance on 1978-06-27. The listed applicant is Great Eastern Lumber Co., Inc.. The 510(k) number is K780999.

When did X-RAY FRAME HOLDER receive FDA 510(k) clearance?

X-RAY FRAME HOLDER received FDA 510(k) clearance on 1978-06-27, under 510(k) number K780999.

Who is the listed applicant for X-RAY FRAME HOLDER?

The FDA 510(k) record lists Great Eastern Lumber Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for X-RAY FRAME HOLDER?

The FDA product code for X-RAY FRAME HOLDER is IZL.

Related Clinical Trials

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Other records listing Great Eastern Lumber Co., 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.

K780708AUTOMATIC RETRACTOR HOLDER

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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