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FDA 510(k)

PROGENY VANTAGE PANORAMIC X-RAY SYSTEM

K-Number: K091866 · 2009-07-20

ApplicantMidmark
Decision Date2009-07-20
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PROGENY VANTAGE PANORAMIC X-RAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Midmark. It received FDA 510(k) clearance on 2009-07-20 under 510(k) number K091866. 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 PROGENY VANTAGE PANORAMIC X-RAY SYSTEM?

PROGENY VANTAGE PANORAMIC X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 2009-07-20. The listed applicant is Midmark. The 510(k) number is K091866.

When did PROGENY VANTAGE PANORAMIC X-RAY SYSTEM receive FDA 510(k) clearance?

PROGENY VANTAGE PANORAMIC X-RAY SYSTEM received FDA 510(k) clearance on 2009-07-20, under 510(k) number K091866.

Who is the listed applicant for PROGENY VANTAGE PANORAMIC X-RAY SYSTEM?

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

What is the FDA product code for PROGENY VANTAGE PANORAMIC X-RAY SYSTEM?

The FDA product code for PROGENY VANTAGE PANORAMIC X-RAY SYSTEM 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 Midmark 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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