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FDA 510(k)

SMS-712NA

K-Number: K903085 · 1990-10-05

ApplicantToshiba America Medical Systems, In.C
Decision Date1990-10-05
Product CodeGXW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SMS-712NA 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 1990-10-05 under 510(k) number K903085. The device is classified under product code GXW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMS-712NA?

SMS-712NA is a medical device that received FDA 510(k) clearance on 1990-10-05. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K903085.

When did SMS-712NA receive FDA 510(k) clearance?

SMS-712NA received FDA 510(k) clearance on 1990-10-05, under 510(k) number K903085.

Who is the listed applicant for SMS-712NA?

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 SMS-712NA?

The FDA product code for SMS-712NA is GXW.

Other records listing Toshiba America Medical Systems, In.C 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.

K132106INFINIX ANGIO WORKSTATION W/DTS SOFTWAREK131822ULTRAEXTEND USWS-900A V2.1 AND V3.1K123097DOSE TRACKING SYSTEM MODEL XIDF-DTS801K122613VANTAGE TITAN WITH HELIOS GRADIENT MODEL MRT-1504/USK121076ULTRAEXTEND FX, ULTRASOUND WORKSTATION PACKAGEK122842RADREX-I, SW V4.00 MODEL DRAD-3000E

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Related Devices (Code: GXW)

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.

K921863SONOS 500, 1000, 1500/SONOS OR ULTRASOUND IMAG SYSHewlett-Packard Co.K8534325.0 IOP & 7.5 IOP PROBESDiasonics, Inc.K833522NEURO SECTOR FIXATION DEVICEAdvanced Technology Laboratories, Inc.K821736ECHO-PULSE KM555Rabar, Inc.K770788ECHOENCEPHALOGRAPH, DIGITAL,DIGIECHO2000Storz Instrument Co.K770575ECHOENCEPHALOGRAPH, DIGITAL, 1000Storz Instrument Co.

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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