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FDA 510(k)

LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS

K-Number: K903160 · 1990-08-08

ApplicantContinental X-Ray Corp.
Decision Date1990-08-08
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS 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 1990-08-08 under 510(k) number K903160. The device is classified under product code IXQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS?

LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS is a medical device that received FDA 510(k) clearance on 1990-08-08. The listed applicant is Continental X-Ray Corp.. The 510(k) number is K903160.

When did LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS receive FDA 510(k) clearance?

LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS received FDA 510(k) clearance on 1990-08-08, under 510(k) number K903160.

Who is the listed applicant for LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS?

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 LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS?

The FDA product code for LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS is IXQ.

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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: IXQ)

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.

K973842CARBON FIBER CONFORMAL COUCH TOPMedtec, Inc.K960083MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300Wuestec Medical, Inc.K954225MED-TEC HAND GRIPMedtec, Inc.K946262EURO, SCST, SCCFT ATLAS RADIOLOGIC TABLESScott Imaging Intl., Inc.K942916OCTOPAQUE UNIVERSALOctostop, Inc.K942190ID100 MOBILE FLUOROSCOPIC EXAMINING TABLEImage Diagnostics, Inc.

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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