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FDA 510(k)

X-RAY POSITIONING DEVICE

K-Number: K770060 · 1977-01-24

ApplicantRobert R. Moore
Decision Date1977-01-24
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-RAY POSITIONING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Robert R. Moore. It received FDA 510(k) clearance on 1977-01-24 under 510(k) number K770060. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-RAY POSITIONING DEVICE?

X-RAY POSITIONING DEVICE is a medical device that received FDA 510(k) clearance on 1977-01-24. The listed applicant is Robert R. Moore. The 510(k) number is K770060.

When did X-RAY POSITIONING DEVICE receive FDA 510(k) clearance?

X-RAY POSITIONING DEVICE received FDA 510(k) clearance on 1977-01-24, under 510(k) number K770060.

Who is the listed applicant for X-RAY POSITIONING DEVICE?

The FDA 510(k) record lists Robert R. Moore as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for X-RAY POSITIONING DEVICE?

The FDA product code for X-RAY POSITIONING DEVICE is KPR.

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 Robert R. Moore 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.

K770658EXERCISER, LEG, LOWER EXTREMITYK770501KNEE CUFF FOR EXPRESSING FLUIDK770223HEAVY FOAM HEEL & ELBOW PROTECTORSK770059ORTHOPEDIC SPECIALTIES

Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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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