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FDA 510(k)

CARDIOCAM MODEL 9CSY0799

K-Number: K011611 · 2001-06-08

ApplicantDanish Diagnostic Development A/S
Decision Date2001-06-08
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CARDIOCAM MODEL 9CSY0799 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 2001-06-08 under 510(k) number K011611. 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 CARDIOCAM MODEL 9CSY0799?

CARDIOCAM MODEL 9CSY0799 is a medical device that received FDA 510(k) clearance on 2001-06-08. The listed applicant is Danish Diagnostic Development A/S. The 510(k) number is K011611.

When did CARDIOCAM MODEL 9CSY0799 receive FDA 510(k) clearance?

CARDIOCAM MODEL 9CSY0799 received FDA 510(k) clearance on 2001-06-08, under 510(k) number K011611.

Who is the listed applicant for CARDIOCAM MODEL 9CSY0799?

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 CARDIOCAM MODEL 9CSY0799?

The FDA product code for CARDIOCAM MODEL 9CSY0799 is KPS.

Related Clinical Trials

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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-ACK040616CARDIOMD-ACK031825C.CAMK001888UNICORN 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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