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FDA 510(k)

CORRIDOR4DM

K-Number: K080575 · 2008-05-13

ApplicantInvia
Decision Date2008-05-13
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CORRIDOR4DM is the device name listed in this FDA 510(k) record. The listed applicant is Invia. It received FDA 510(k) clearance on 2008-05-13 under 510(k) number K080575. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORRIDOR4DM?

CORRIDOR4DM is a medical device that received FDA 510(k) clearance on 2008-05-13. The listed applicant is Invia. The 510(k) number is K080575.

When did CORRIDOR4DM receive FDA 510(k) clearance?

CORRIDOR4DM received FDA 510(k) clearance on 2008-05-13, under 510(k) number K080575.

Who is the listed applicant for CORRIDOR4DM?

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

What is the FDA product code for CORRIDOR4DM?

The FDA product code for CORRIDOR4DM is KPS.

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 Invia 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.

K101279CORRIDOR4DM V2010 MODEL: V2010

Related Devices (Code: KPS)

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.

K261305MICSI-PETMicrostructure Imaging, Inc.K261427uMI Panvivo (uMI Panvivo M)Shanghai United Imaging Healthcare Co., Ltd.K261315Symbia Pro.specta Q3 (11364751);Symbia Pro.specta X3 (11364752);Symbia Pro.specta X7 (11364753);Symbia Pro.specta VA40 FamilySiemens Medical Solutions USA, Inc.K260524uMI Panvivo (uMI Panvivo LS); uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES)Shanghai United Imaging Healthcare Co., Ltd.K253564uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES)Shanghai United Imaging Healthcare Co., Ltd.K254001VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464)Spectrum Dynamics Medical, Ltd.

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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