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FDA 510(k)

MULTICAM 3000 ECO

K-Number: K132347 · 2013-11-20

ApplicantInter Medical Medizintechnik GmbH
Decision Date2013-11-20
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTICAM 3000 ECO is the device name listed in this FDA 510(k) record. The listed applicant is Inter Medical Medizintechnik GmbH. It received FDA 510(k) clearance on 2013-11-20 under 510(k) number K132347. 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 MULTICAM 3000 ECO?

MULTICAM 3000 ECO is a medical device that received FDA 510(k) clearance on 2013-11-20. The listed applicant is Inter Medical Medizintechnik GmbH. The 510(k) number is K132347.

When did MULTICAM 3000 ECO receive FDA 510(k) clearance?

MULTICAM 3000 ECO received FDA 510(k) clearance on 2013-11-20, under 510(k) number K132347.

Who is the listed applicant for MULTICAM 3000 ECO?

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

What is the FDA product code for MULTICAM 3000 ECO?

The FDA product code for MULTICAM 3000 ECO 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 Inter Medical Medizintechnik GmbH 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.

K230393UniCam Evo SoftwareK052473CX 250 C PLUS WITH GAMMAXP SOFTWARE, MODEL 0121 0000

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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