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FDA 510(k)

X-RAY EQUIPMENT (VARIOUS TYPES)

K-Number: K895730 · 1989-11-06

ApplicantContinental X-Ray Corp.
Decision Date1989-11-06
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-RAY EQUIPMENT (VARIOUS TYPES) 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 1989-11-06 under 510(k) number K895730. 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 X-RAY EQUIPMENT (VARIOUS TYPES)?

X-RAY EQUIPMENT (VARIOUS TYPES) is a medical device that received FDA 510(k) clearance on 1989-11-06. The listed applicant is Continental X-Ray Corp.. The 510(k) number is K895730.

When did X-RAY EQUIPMENT (VARIOUS TYPES) receive FDA 510(k) clearance?

X-RAY EQUIPMENT (VARIOUS TYPES) received FDA 510(k) clearance on 1989-11-06, under 510(k) number K895730.

Who is the listed applicant for X-RAY EQUIPMENT (VARIOUS TYPES)?

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 X-RAY EQUIPMENT (VARIOUS TYPES)?

The FDA product code for X-RAY EQUIPMENT (VARIOUS TYPES) 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.

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

View all 27 devices →

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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