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FDA 510(k)

MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAY

K-Number: K874238 · 1987-12-07

Decision Date1987-12-07
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL 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 1987-12-07 under 510(k) number K874238. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAY?

MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAY is a medical device that received FDA 510(k) clearance on 1987-12-07. The listed applicant is Belmont Equipment Corp.. The 510(k) number is K874238.

When did MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAY receive FDA 510(k) clearance?

MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAY received FDA 510(k) clearance on 1987-12-07, under 510(k) number K874238.

Who is the listed applicant for MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL 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 MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAY?

The FDA product code for MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAY is EHD.

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.

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.

View all 12 devices →

Related Devices (Code: EHD)

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.

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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