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FDA 510(k)

MTV-250A, MTV-300A

K-Number: K924478 · 1992-12-04

ApplicantToshiba America Medical Systems, In.C
Decision Date1992-12-04
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MTV-250A, MTV-300A 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 1992-12-04 under 510(k) number K924478. The device is classified under product code LMA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTV-250A, MTV-300A?

MTV-250A, MTV-300A is a medical device that received FDA 510(k) clearance on 1992-12-04. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K924478.

When did MTV-250A, MTV-300A receive FDA 510(k) clearance?

MTV-250A, MTV-300A received FDA 510(k) clearance on 1992-12-04, under 510(k) number K924478.

Who is the listed applicant for MTV-250A, MTV-300A?

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 MTV-250A, MTV-300A?

The FDA product code for MTV-250A, MTV-300A is LMA.

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

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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: LMA)

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.

K132183DICOM VIDEOBar Code Computer, Ltd.K130636TELERADPRO EDGE; TELERADPRO EDGE HD-CCDVidar Systems Corp.K130406DIAGNOSTICPRO EDGEVidar Systems Corp.K102476TELERADPROVidar Systems Corp.K093809VIDAR DENTAL FILM DIGITIZERVidar Systems Corp.K091288MEDI-6000 MEDICAL IMAGE DIGITIZERMicrotek International, 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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