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FDA 510(k)

MULTIX U. BUCKY TABLE X-RAY UNIT

K-Number: K803130 · 1981-01-28

ApplicantSiemens Corp.
Decision Date1981-01-28
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTIX U. BUCKY TABLE X-RAY UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1981-01-28 under 510(k) number K803130. 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 U. BUCKY TABLE X-RAY UNIT?

MULTIX U. BUCKY TABLE X-RAY UNIT is a medical device that received FDA 510(k) clearance on 1981-01-28. The listed applicant is Siemens Corp.. The 510(k) number is K803130.

When did MULTIX U. BUCKY TABLE X-RAY UNIT receive FDA 510(k) clearance?

MULTIX U. BUCKY TABLE X-RAY UNIT received FDA 510(k) clearance on 1981-01-28, under 510(k) number K803130.

Who is the listed applicant for MULTIX U. BUCKY TABLE X-RAY UNIT?

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

What is the FDA product code for MULTIX U. BUCKY TABLE X-RAY UNIT?

The FDA product code for MULTIX U. BUCKY TABLE X-RAY UNIT 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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