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FDA 510(k)

ALPHARD CONE BEAM CT, MODEL X178

K-Number: K072574 · 2007-10-18

ApplicantTakara Belmont Corp.
Decision Date2007-10-18
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ALPHARD CONE BEAM CT, MODEL X178 is the device name listed in this FDA 510(k) record. The listed applicant is Takara Belmont Corp.. It received FDA 510(k) clearance on 2007-10-18 under 510(k) number K072574. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALPHARD CONE BEAM CT, MODEL X178?

ALPHARD CONE BEAM CT, MODEL X178 is a medical device that received FDA 510(k) clearance on 2007-10-18. The listed applicant is Takara Belmont Corp.. The 510(k) number is K072574.

When did ALPHARD CONE BEAM CT, MODEL X178 receive FDA 510(k) clearance?

ALPHARD CONE BEAM CT, MODEL X178 received FDA 510(k) clearance on 2007-10-18, under 510(k) number K072574.

Who is the listed applicant for ALPHARD CONE BEAM CT, MODEL X178?

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

What is the FDA product code for ALPHARD CONE BEAM CT, MODEL X178?

The FDA product code for ALPHARD CONE BEAM CT, MODEL X178 is JAK.

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.

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Other records listing Takara Belmont 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.

K101181BEL-CATK093240BELRAY II

Related Devices (Code: JAK)

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.

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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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