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FDA 510(k)

MULTIX FUSION

K-Number: K121513 · 2012-08-10

ApplicantSiemens Medical Solution
Decision Date2012-08-10
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTIX FUSION is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solution. It received FDA 510(k) clearance on 2012-08-10 under 510(k) number K121513. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIX FUSION?

MULTIX FUSION is a medical device that received FDA 510(k) clearance on 2012-08-10. The listed applicant is Siemens Medical Solution. The 510(k) number is K121513.

When did MULTIX FUSION receive FDA 510(k) clearance?

MULTIX FUSION received FDA 510(k) clearance on 2012-08-10, under 510(k) number K121513.

Who is the listed applicant for MULTIX FUSION?

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

What is the FDA product code for MULTIX FUSION?

The FDA product code for MULTIX FUSION is KPR.

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Other records listing Siemens Medical Solution 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.

K121138ACUSON S3000 DIAGNOSTIC ULTRASOUND SYSTEMK061449SYNGO EXPERT-1K050199MAGNETOM SYMPHONY A TIM SYSTEM

Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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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