FDA 510(k)

OMNIFLEX OVERHEAD TUBECRANE CAT.#S-9108/#6713.400

K-Number: K913121 · 1991-08-16

Decision Date1991-08-16

Product CodeKXJ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

OMNIFLEX OVERHEAD TUBECRANE CAT.#S-9108/#6713.400 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 1991-08-16 under 510(k) number K913121. The device is classified under product code KXJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMNIFLEX OVERHEAD TUBECRANE CAT.#S-9108/#6713.400?

OMNIFLEX OVERHEAD TUBECRANE CAT.#S-9108/#6713.400 is a medical device that received FDA 510(k) clearance on 1991-08-16. The listed applicant is Continental X-Ray Corp.. The 510(k) number is K913121.

When did OMNIFLEX OVERHEAD TUBECRANE CAT.#S-9108/#6713.400 receive FDA 510(k) clearance?

OMNIFLEX OVERHEAD TUBECRANE CAT.#S-9108/#6713.400 received FDA 510(k) clearance on 1991-08-16, under 510(k) number K913121.

Who is the listed applicant for OMNIFLEX OVERHEAD TUBECRANE CAT.#S-9108/#6713.400?

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 OMNIFLEX OVERHEAD TUBECRANE CAT.#S-9108/#6713.400?

The FDA product code for OMNIFLEX OVERHEAD TUBECRANE CAT.#S-9108/#6713.400 is KXJ.

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Other records listing Continental X-Ray Corp. as applicant

K972442CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002 K962140ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300 K961690CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105 K954581ARC SERIES K950571LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270 K942175LINEAR TOMOGRAPHIC SYSTEM: PMT 6000

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Related Devices (Code: KXJ)

K050190APOLLOVilla Sistemi Medicali S.P.A.K963905RADIOGRAPHIC ITT TABLEX-Ray Technologies, Inc.K955414XRT 400Wuestec Medical, Inc.K951146IMAGING TABLESepta Corp.K950068CARBON FIBER COUCH INSERTMedtec, Inc.K950442INFRARED EXPOSURE HAND SWITCHMedical X-Ray Intl., 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.