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FDA 510(k)

PANORAMIC MODEL X-CALIBER X-RAY

K-Number: K900681 · 1990-05-23

Decision Date1990-05-23
Product CodeEAP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PANORAMIC MODEL X-CALIBER 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 1990-05-23 under 510(k) number K900681. 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 PANORAMIC MODEL X-CALIBER X-RAY?

PANORAMIC MODEL X-CALIBER X-RAY is a medical device that received FDA 510(k) clearance on 1990-05-23. The listed applicant is Belmont Equipment Corp.. The 510(k) number is K900681.

When did PANORAMIC MODEL X-CALIBER X-RAY receive FDA 510(k) clearance?

PANORAMIC MODEL X-CALIBER X-RAY received FDA 510(k) clearance on 1990-05-23, under 510(k) number K900681.

Who is the listed applicant for PANORAMIC MODEL X-CALIBER 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 PANORAMIC MODEL X-CALIBER X-RAY?

The FDA product code for PANORAMIC MODEL X-CALIBER X-RAY 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.

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: 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.

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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