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FDA 510(k)

ENCOMPASS HF100- EAGLE PANORAMIC/CEPHALOMETRIC X-RAY

K-Number: K110371 · 2011-03-17

Decision Date2011-03-17
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENCOMPASS HF100- EAGLE PANORAMIC/CEPHALOMETRIC X-RAY is the device name listed in this FDA 510(k) record. The listed applicant is Panoramic Corp.. It received FDA 510(k) clearance on 2011-03-17 under 510(k) number K110371. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENCOMPASS HF100- EAGLE PANORAMIC/CEPHALOMETRIC X-RAY?

ENCOMPASS HF100- EAGLE PANORAMIC/CEPHALOMETRIC X-RAY is a medical device that received FDA 510(k) clearance on 2011-03-17. The listed applicant is Panoramic Corp.. The 510(k) number is K110371.

When did ENCOMPASS HF100- EAGLE PANORAMIC/CEPHALOMETRIC X-RAY receive FDA 510(k) clearance?

ENCOMPASS HF100- EAGLE PANORAMIC/CEPHALOMETRIC X-RAY received FDA 510(k) clearance on 2011-03-17, under 510(k) number K110371.

Who is the listed applicant for ENCOMPASS HF100- EAGLE PANORAMIC/CEPHALOMETRIC X-RAY?

The FDA 510(k) record lists Panoramic Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENCOMPASS HF100- EAGLE PANORAMIC/CEPHALOMETRIC X-RAY?

The FDA product code for ENCOMPASS HF100- EAGLE PANORAMIC/CEPHALOMETRIC X-RAY is MUH.

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 Panoramic 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.

Related Devices (Code: MUH)

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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