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FDA 510(k)

TILTING IMAGING TABLE #846T

K-Number: K803120 · 1981-01-22

ApplicantQuinton, Inc.
Decision Date1981-01-22
Product CodeKXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TILTING IMAGING TABLE #846T is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1981-01-22 under 510(k) number K803120. 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 TILTING IMAGING TABLE #846T?

TILTING IMAGING TABLE #846T is a medical device that received FDA 510(k) clearance on 1981-01-22. The listed applicant is Quinton, Inc.. The 510(k) number is K803120.

When did TILTING IMAGING TABLE #846T receive FDA 510(k) clearance?

TILTING IMAGING TABLE #846T received FDA 510(k) clearance on 1981-01-22, under 510(k) number K803120.

Who is the listed applicant for TILTING IMAGING TABLE #846T?

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

What is the FDA product code for TILTING IMAGING TABLE #846T?

The FDA product code for TILTING IMAGING TABLE #846T is KXJ.

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Other records listing Quinton, Inc. as applicant

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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.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.

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