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FDA 510(k)

BUCKY STAND BR-10M

K-Number: K942792 · 1994-07-29

ApplicantShimadzu Corp.
Decision Date1994-07-29
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BUCKY STAND BR-10M is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Corp.. It received FDA 510(k) clearance on 1994-07-29 under 510(k) number K942792. 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 BUCKY STAND BR-10M?

BUCKY STAND BR-10M is a medical device that received FDA 510(k) clearance on 1994-07-29. The listed applicant is Shimadzu Corp.. The 510(k) number is K942792.

When did BUCKY STAND BR-10M receive FDA 510(k) clearance?

BUCKY STAND BR-10M received FDA 510(k) clearance on 1994-07-29, under 510(k) number K942792.

Who is the listed applicant for BUCKY STAND BR-10M?

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

What is the FDA product code for BUCKY STAND BR-10M?

The FDA product code for BUCKY STAND BR-10M is KPR.

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Other records listing Shimadzu Corp. 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.

K101039SHIMADZU COLLIMATOR R-300K101036SHIMADZU COLLIMATOR R-20JK090578SHIMADZU COLLIMATOR R-30HK090268SHIMADZU MOBILE X-RAY SYSTEM MOBILE ART EVOLUTIONK080701SHIMADZU MOBILE X-RAY SYSTEM MOBILEDART EVOLUTIONK072006DAR-9400F

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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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