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FDA 510(k)

SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150B

K-Number: K884477 · 1989-03-15

ApplicantShimadzu Precision Instruments, Inc.
Decision Date1989-03-15
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150B is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Precision Instruments, Inc.. It received FDA 510(k) clearance on 1989-03-15 under 510(k) number K884477. 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 SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150B?

SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150B is a medical device that received FDA 510(k) clearance on 1989-03-15. The listed applicant is Shimadzu Precision Instruments, Inc.. The 510(k) number is K884477.

When did SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150B receive FDA 510(k) clearance?

SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150B received FDA 510(k) clearance on 1989-03-15, under 510(k) number K884477.

Who is the listed applicant for SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150B?

The FDA 510(k) record lists Shimadzu Precision Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150B?

The FDA product code for SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150B is KPR.

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Other records listing Shimadzu Precision Instruments, Inc. 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.

K940294SHIMADZU MOBILE X-RAY SYSTEMSK890913SDU 800 DIAGNOSTIC ULTRASOUND INSTRUMENTK884598SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-1200K875378SINGLE PHOTON SET 031 & AZ-701-NTS-SP EMISSIONK882311SHIMADZU LATERAL C-ARM MH-31K881674SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TC

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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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