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FDA 510(k)

RADIOGRAPHIC ITT TABLE

K-Number: K963905 · 1996-11-12

ApplicantX-Ray Technologies, Inc.
Decision Date1996-11-12
Product CodeKXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIOGRAPHIC ITT TABLE is the device name listed in this FDA 510(k) record. The listed applicant is X-Ray Technologies, Inc.. It received FDA 510(k) clearance on 1996-11-12 under 510(k) number K963905. 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 RADIOGRAPHIC ITT TABLE?

RADIOGRAPHIC ITT TABLE is a medical device that received FDA 510(k) clearance on 1996-11-12. The listed applicant is X-Ray Technologies, Inc.. The 510(k) number is K963905.

When did RADIOGRAPHIC ITT TABLE receive FDA 510(k) clearance?

RADIOGRAPHIC ITT TABLE received FDA 510(k) clearance on 1996-11-12, under 510(k) number K963905.

Who is the listed applicant for RADIOGRAPHIC ITT TABLE?

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

What is the FDA product code for RADIOGRAPHIC ITT TABLE?

The FDA product code for RADIOGRAPHIC ITT TABLE is KXJ.

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Related Devices (Code: KXJ)

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.

K050190APOLLOVilla Sistemi Medicali S.P.A.K955414XRT 400Wuestec Medical, Inc.K951146IMAGING TABLESepta Corp.K950068CARBON FIBER COUCH INSERTMedtec, Inc.K950442INFRARED EXPOSURE HAND SWITCHMedical X-Ray Intl., Inc.K940696SYNCRA TILT OPTION FOR ANGIO DIAGNOST 5Philips Medical Systems North America, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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