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FDA 510(k)

MINICAT DENTOCAT

K-Number: K032243 · 2003-10-02

ApplicantXoran Technologies, Inc.
Decision Date2003-10-02
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MINICAT DENTOCAT is the device name listed in this FDA 510(k) record. The listed applicant is Xoran Technologies, Inc.. It received FDA 510(k) clearance on 2003-10-02 under 510(k) number K032243. 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 MINICAT DENTOCAT?

MINICAT DENTOCAT is a medical device that received FDA 510(k) clearance on 2003-10-02. The listed applicant is Xoran Technologies, Inc.. The 510(k) number is K032243.

When did MINICAT DENTOCAT receive FDA 510(k) clearance?

MINICAT DENTOCAT received FDA 510(k) clearance on 2003-10-02, under 510(k) number K032243.

Who is the listed applicant for MINICAT DENTOCAT?

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

What is the FDA product code for MINICAT DENTOCAT?

The FDA product code for MINICAT DENTOCAT 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 Xoran Technologies, Inc. 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.

K113421MINICATK073306XORANCONNECTK061834XCAT; XCAT FOR NEURO

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.

K261125BodyTom 64 (NL4100); OmniTom Elite (NL5000)Samsung HME America, Inc., dba NeuroLogica Corp.K261229SCENARIA View Phase 6.0Fujifilm CorporationK253836FCT iStream Phase 2Fujifilm CorporationK253450BodyTom Elite (NL4000)NeuroLogica Corp., a Samsung CompanyK253770CardIQ SuiteGE Medical Systems SCSK253560Enhanced Boundary for PCCTGe Medical Systems, LLC

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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