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FDA 510(k)

SXT-60F/60M MOBILE C ARM X-RAY UNIT

K-Number: K896387 · 1990-02-23

ApplicantToshiba America Medical Systems, In.C
Decision Date1990-02-23
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SXT-60F/60M MOBILE C ARM X-RAY UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Medical Systems, In.C. It received FDA 510(k) clearance on 1990-02-23 under 510(k) number K896387. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SXT-60F/60M MOBILE C ARM X-RAY UNIT?

SXT-60F/60M MOBILE C ARM X-RAY UNIT is a medical device that received FDA 510(k) clearance on 1990-02-23. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K896387.

When did SXT-60F/60M MOBILE C ARM X-RAY UNIT receive FDA 510(k) clearance?

SXT-60F/60M MOBILE C ARM X-RAY UNIT received FDA 510(k) clearance on 1990-02-23, under 510(k) number K896387.

Who is the listed applicant for SXT-60F/60M MOBILE C ARM X-RAY UNIT?

The FDA 510(k) record lists Toshiba America Medical Systems, In.C as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SXT-60F/60M MOBILE C ARM X-RAY UNIT?

The FDA product code for SXT-60F/60M MOBILE C ARM X-RAY UNIT is OXO.

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Related Devices (Code: OXO)

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.

K253296Digital C-ARM with 3DAllengers Medical Systems LimitedK252579Orthoscan TAU MVP Mini C-Arm SystemZiehm-Orthoscan, Inc.K253269OEC One CFDGe Hualun Medical Systems Co. , Ltd.K251004Dual-Mode Mobile C-Arm (Geelin500A, Geelin500M)Hefei Chimed Intelligent Machine Co., Ltd.K250587Orthoscan TAU Mini C-ArmZiehm-Orthoscan, Inc.K243452Orthoscan VERSA Mini C-ArmZiehm-Orthoscan, 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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