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FDA 510(k)

BELMONT PODIATRY MODEL 065 X-RAY

K-Number: K811142 · 1981-06-09

ApplicantBelmont Equipment Corp.
Decision Date1981-06-09
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BELMONT PODIATRY MODEL 065 X-RAY is the device name listed in this FDA 510(k) record. The listed applicant is Belmont Equipment Corp.. It received FDA 510(k) clearance on 1981-06-09 under 510(k) number K811142. 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 BELMONT PODIATRY MODEL 065 X-RAY?

BELMONT PODIATRY MODEL 065 X-RAY is a medical device that received FDA 510(k) clearance on 1981-06-09. The listed applicant is Belmont Equipment Corp.. The 510(k) number is K811142.

When did BELMONT PODIATRY MODEL 065 X-RAY receive FDA 510(k) clearance?

BELMONT PODIATRY MODEL 065 X-RAY received FDA 510(k) clearance on 1981-06-09, under 510(k) number K811142.

Who is the listed applicant for BELMONT PODIATRY MODEL 065 X-RAY?

The FDA 510(k) record lists Belmont Equipment Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BELMONT PODIATRY MODEL 065 X-RAY?

The FDA product code for BELMONT PODIATRY MODEL 065 X-RAY 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 Belmont Equipment Corp. 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.

K000799BELMONT UNIT, MODEL 2000 SERIESK983661BELMONT UNIT, MODEL 6000 SERIES AND 7500 SERIESK963699BELRAY/MODEL 096, DENTAL INTRAORAL X-RAYK900681PANORAMIC MODEL X-CALIBER X-RAYK874238MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAYK870300BELMONT, PODIATRY X-RAY - REMEX, MODEL PD75

View all 12 devices →

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

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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