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FDA 510(k)

CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002

K-Number: K972442 · 1997-09-11

ApplicantContinental X-Ray Corp.
Decision Date1997-09-11
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002 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 1997-09-11 under 510(k) number K972442. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002?

CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002 is a medical device that received FDA 510(k) clearance on 1997-09-11. The listed applicant is Continental X-Ray Corp.. The 510(k) number is K972442.

When did CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002 receive FDA 510(k) clearance?

CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002 received FDA 510(k) clearance on 1997-09-11, under 510(k) number K972442.

Who is the listed applicant for CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002?

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 CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002?

The FDA product code for CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002 is JAA.

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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.

K962140ICT-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 6000K942100MODEL TM EP HIGH VOLTAGE GENERATOR

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Related Devices (Code: JAA)

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.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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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