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FDA 510(k)

SHIMADZU CEILING TUBE SUPPORT CH-30GH

K-Number: K990715 · 1999-04-16

ApplicantShimadzu Corp.
Decision Date1999-04-16
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SHIMADZU CEILING TUBE SUPPORT CH-30GH is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Corp.. It received FDA 510(k) clearance on 1999-04-16 under 510(k) number K990715. 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 CEILING TUBE SUPPORT CH-30GH?

SHIMADZU CEILING TUBE SUPPORT CH-30GH is a medical device that received FDA 510(k) clearance on 1999-04-16. The listed applicant is Shimadzu Corp.. The 510(k) number is K990715.

When did SHIMADZU CEILING TUBE SUPPORT CH-30GH receive FDA 510(k) clearance?

SHIMADZU CEILING TUBE SUPPORT CH-30GH received FDA 510(k) clearance on 1999-04-16, under 510(k) number K990715.

Who is the listed applicant for SHIMADZU CEILING TUBE SUPPORT CH-30GH?

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 SHIMADZU CEILING TUBE SUPPORT CH-30GH?

The FDA product code for SHIMADZU CEILING TUBE SUPPORT CH-30GH 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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