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FDA 510(k)

WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY

K-Number: K935649 · 1994-02-09

ApplicantBennett X-Ray Corp.
Decision Date1994-02-09
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY is the device name listed in this FDA 510(k) record. The listed applicant is Bennett X-Ray Corp.. It received FDA 510(k) clearance on 1994-02-09 under 510(k) number K935649. 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 WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY?

WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY is a medical device that received FDA 510(k) clearance on 1994-02-09. The listed applicant is Bennett X-Ray Corp.. The 510(k) number is K935649.

When did WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY receive FDA 510(k) clearance?

WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY received FDA 510(k) clearance on 1994-02-09, under 510(k) number K935649.

Who is the listed applicant for WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY?

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

What is the FDA product code for WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY?

The FDA product code for WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY is KPR.

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Other records listing Bennett X-Ray 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.

K964576PROFILE MAMMOGRAPHY SYSTEM (M-PRO)K952672VERTICAL INTEGRATED PERFECT VIEW (VIP) RADIOGRAPHIC SYSTEMK944978BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSIK945962BENNETT X-RAY PROFILE POSITIONING PADDLE FOR MAMMOGRAPHYK945749BENNETT X-RAY TOMOGRAPHY SYSTEMK945731HFQ HIGH FREQUENCY RADIOGRAPHIC AND FLUROSCOPIC GENERATORS

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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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