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FDA 510(k)

BELRAY/MODEL 096, DENTAL INTRAORAL X-RAY

K-Number: K963699 · 1996-12-23

Decision Date1996-12-23
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BELRAY/MODEL 096, 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 1996-12-23 under 510(k) number K963699. 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 BELRAY/MODEL 096, DENTAL INTRAORAL X-RAY?

BELRAY/MODEL 096, DENTAL INTRAORAL X-RAY is a medical device that received FDA 510(k) clearance on 1996-12-23. The listed applicant is Belmont Equipment Corp.. The 510(k) number is K963699.

When did BELRAY/MODEL 096, DENTAL INTRAORAL X-RAY receive FDA 510(k) clearance?

BELRAY/MODEL 096, DENTAL INTRAORAL X-RAY received FDA 510(k) clearance on 1996-12-23, under 510(k) number K963699.

Who is the listed applicant for BELRAY/MODEL 096, 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 BELRAY/MODEL 096, DENTAL INTRAORAL X-RAY?

The FDA product code for BELRAY/MODEL 096, 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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