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FDA 510(k)

BELMONT, PODIATRY X-RAY - REMEX, MODEL PD75

K-Number: K870300 · 1987-03-25

ApplicantBelmont Equipment Corp.
Decision Date1987-03-25
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BELMONT, PODIATRY X-RAY - REMEX, MODEL PD75 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 1987-03-25 under 510(k) number K870300. 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 X-RAY - REMEX, MODEL PD75?

BELMONT, PODIATRY X-RAY - REMEX, MODEL PD75 is a medical device that received FDA 510(k) clearance on 1987-03-25. The listed applicant is Belmont Equipment Corp.. The 510(k) number is K870300.

When did BELMONT, PODIATRY X-RAY - REMEX, MODEL PD75 receive FDA 510(k) clearance?

BELMONT, PODIATRY X-RAY - REMEX, MODEL PD75 received FDA 510(k) clearance on 1987-03-25, under 510(k) number K870300.

Who is the listed applicant for BELMONT, PODIATRY X-RAY - REMEX, MODEL PD75?

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 X-RAY - REMEX, MODEL PD75?

The FDA product code for BELMONT, PODIATRY X-RAY - REMEX, MODEL PD75 is KPR.

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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-RAYK861328NEW BELMONT MODEL, MC-5 DENTAL, INTRAORAL X-RAY

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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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