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FDA 510(k)

IMAGING TABLE

K-Number: K951146 · 1995-05-04

ApplicantSepta Corp.
Decision Date1995-05-04
Product CodeKXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMAGING TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Septa Corp.. It received FDA 510(k) clearance on 1995-05-04 under 510(k) number K951146. 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 IMAGING TABLE?

IMAGING TABLE is a medical device that received FDA 510(k) clearance on 1995-05-04. The listed applicant is Septa Corp.. The 510(k) number is K951146.

When did IMAGING TABLE receive FDA 510(k) clearance?

IMAGING TABLE received FDA 510(k) clearance on 1995-05-04, under 510(k) number K951146.

Who is the listed applicant for IMAGING TABLE?

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

What is the FDA product code for IMAGING TABLE?

The FDA product code for IMAGING 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.K963905RADIOGRAPHIC ITT TABLEX-Ray Technologies, Inc.K955414XRT 400Wuestec Medical, Inc.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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