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FDA 510(k)

REMOTE-CONTROLLED UNIVERSAL DIAG. TABLE RS-100

K-Number: K874639 · 1987-12-04

ApplicantShimadzu Precision Instruments, Inc.
Decision Date1987-12-04
Product CodeKXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

REMOTE-CONTROLLED UNIVERSAL DIAG. TABLE RS-100 is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Precision Instruments, Inc.. It received FDA 510(k) clearance on 1987-12-04 under 510(k) number K874639. 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 REMOTE-CONTROLLED UNIVERSAL DIAG. TABLE RS-100?

REMOTE-CONTROLLED UNIVERSAL DIAG. TABLE RS-100 is a medical device that received FDA 510(k) clearance on 1987-12-04. The listed applicant is Shimadzu Precision Instruments, Inc.. The 510(k) number is K874639.

When did REMOTE-CONTROLLED UNIVERSAL DIAG. TABLE RS-100 receive FDA 510(k) clearance?

REMOTE-CONTROLLED UNIVERSAL DIAG. TABLE RS-100 received FDA 510(k) clearance on 1987-12-04, under 510(k) number K874639.

Who is the listed applicant for REMOTE-CONTROLLED UNIVERSAL DIAG. TABLE RS-100?

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

What is the FDA product code for REMOTE-CONTROLLED UNIVERSAL DIAG. TABLE RS-100?

The FDA product code for REMOTE-CONTROLLED UNIVERSAL DIAG. TABLE RS-100 is KXJ.

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Other records listing Shimadzu Precision Instruments, Inc. 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.

K940294SHIMADZU MOBILE X-RAY SYSTEMSK890913SDU 800 DIAGNOSTIC ULTRASOUND INSTRUMENTK884598SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-1200K884477SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150BK875378SINGLE PHOTON SET 031 & AZ-701-NTS-SP EMISSIONK882311SHIMADZU LATERAL C-ARM MH-31

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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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