FDA 510(k)

BEL-CAT

K-Number: K101181 · 2011-07-19

Decision Date2011-07-19

Product CodeOAS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

BEL-CAT 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 2011-07-19 under 510(k) number K101181. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEL-CAT?

BEL-CAT is a medical device that received FDA 510(k) clearance on 2011-07-19. The listed applicant is Takara Belmont Corp.. The 510(k) number is K101181.

When did BEL-CAT receive FDA 510(k) clearance?

BEL-CAT received FDA 510(k) clearance on 2011-07-19, under 510(k) number K101181.

Who is the listed applicant for BEL-CAT?

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 BEL-CAT?

The FDA product code for BEL-CAT is OAS.

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.

K093240BELRAY II K072574ALPHARD CONE BEAM CT, MODEL X178

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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.