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FDA 510(k)

BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD

K-Number: K852019 · 1985-06-05

ApplicantBelmont Equipment Corp.
Decision Date1985-06-05
Product CodeEAP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD 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 1985-06-05 under 510(k) number K852019. The device is classified under product code EAP. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD?

BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD is a medical device that received FDA 510(k) clearance on 1985-06-05. The listed applicant is Belmont Equipment Corp.. The 510(k) number is K852019.

When did BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD receive FDA 510(k) clearance?

BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD received FDA 510(k) clearance on 1985-06-05, under 510(k) number K852019.

Who is the listed applicant for BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD?

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 AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD?

The FDA product code for BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD is EAP.

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: EAP)

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.

K113360MEDICAL IMAGE PROCESSING UNITHumanray Co,LtdK102573PROVU (TM) DENTAL X-RAY SYSTEMAdvanced Image Science, Inc.K093453MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEMSchick Technologies, Inc.K080738DENTRON SENSORDentron Systems, LLCK052422THE ENVISION INTRAORAL DENTAL X-RAY MACHINES (WALL MOUNTED AND MOBILE)Flow X-Ray Corp.K041385MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEMSchick Technologies, Inc.

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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