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FDA 510(k)

FLOOR MOUNT TUBESTAND PERFORMER, 6610.101/S-9109

K-Number: K912517 · 1991-09-19

ApplicantContinental X-Ray Corp.
Decision Date1991-09-19
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FLOOR MOUNT TUBESTAND PERFORMER, 6610.101/S-9109 is the device name listed in this FDA 510(k) record. The listed applicant is Continental X-Ray Corp.. It received FDA 510(k) clearance on 1991-09-19 under 510(k) number K912517. 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 FLOOR MOUNT TUBESTAND PERFORMER, 6610.101/S-9109?

FLOOR MOUNT TUBESTAND PERFORMER, 6610.101/S-9109 is a medical device that received FDA 510(k) clearance on 1991-09-19. The listed applicant is Continental X-Ray Corp.. The 510(k) number is K912517.

When did FLOOR MOUNT TUBESTAND PERFORMER, 6610.101/S-9109 receive FDA 510(k) clearance?

FLOOR MOUNT TUBESTAND PERFORMER, 6610.101/S-9109 received FDA 510(k) clearance on 1991-09-19, under 510(k) number K912517.

Who is the listed applicant for FLOOR MOUNT TUBESTAND PERFORMER, 6610.101/S-9109?

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

What is the FDA product code for FLOOR MOUNT TUBESTAND PERFORMER, 6610.101/S-9109?

The FDA product code for FLOOR MOUNT TUBESTAND PERFORMER, 6610.101/S-9109 is KPR.

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Other records listing Continental 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.

K972442CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002K962140ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300K961690CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105K954581ARC SERIESK950571LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270K942175LINEAR TOMOGRAPHIC SYSTEM: PMT 6000

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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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