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FDA 510(k)

CARDIOMD-AC

K-Number: K040616 · 2004-03-24

ApplicantDanish Diagnostic Development A/S
Decision Date2004-03-24
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CARDIOMD-AC is the device name listed in this FDA 510(k) record. The listed applicant is Danish Diagnostic Development A/S. It received FDA 510(k) clearance on 2004-03-24 under 510(k) number K040616. 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 CARDIOMD-AC?

CARDIOMD-AC is a medical device that received FDA 510(k) clearance on 2004-03-24. The listed applicant is Danish Diagnostic Development A/S. The 510(k) number is K040616.

When did CARDIOMD-AC receive FDA 510(k) clearance?

CARDIOMD-AC received FDA 510(k) clearance on 2004-03-24, under 510(k) number K040616.

Who is the listed applicant for CARDIOMD-AC?

The FDA 510(k) record lists Danish Diagnostic Development A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARDIOMD-AC?

The FDA product code for CARDIOMD-AC 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 Danish Diagnostic Development A/S 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.

K081829CAPIMAGEK051460C.CAM-ACK031825C.CAMK011611CARDIOCAM MODEL 9CSY0799K001888UNICORN MODEL SYS0630

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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