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FDA 510(k)

MULTIX COMPACT K AND MULTIX L RADIOGRAPHIC X-RAY SYSTEMS

K-Number: K001201 · 2000-06-01

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2000-06-01
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTIX COMPACT K AND MULTIX L RADIOGRAPHIC X-RAY SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2000-06-01 under 510(k) number K001201. 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 COMPACT K AND MULTIX L RADIOGRAPHIC X-RAY SYSTEMS?

MULTIX COMPACT K AND MULTIX L RADIOGRAPHIC X-RAY SYSTEMS is a medical device that received FDA 510(k) clearance on 2000-06-01. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K001201.

When did MULTIX COMPACT K AND MULTIX L RADIOGRAPHIC X-RAY SYSTEMS receive FDA 510(k) clearance?

MULTIX COMPACT K AND MULTIX L RADIOGRAPHIC X-RAY SYSTEMS received FDA 510(k) clearance on 2000-06-01, under 510(k) number K001201.

Who is the listed applicant for MULTIX COMPACT K AND MULTIX L RADIOGRAPHIC X-RAY SYSTEMS?

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

What is the FDA product code for MULTIX COMPACT K AND MULTIX L RADIOGRAPHIC X-RAY SYSTEMS?

The FDA product code for MULTIX COMPACT K AND MULTIX L RADIOGRAPHIC X-RAY SYSTEMS is KPR.

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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