FDA 510(k)

GCA-7200A

K-Number: K931297 · 1993-07-27

ApplicantToshiba America Medical Systems, In.C

Decision Date1993-07-27

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

GCA-7200A 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 1993-07-27 under 510(k) number K931297. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GCA-7200A?

GCA-7200A is a medical device that received FDA 510(k) clearance on 1993-07-27. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K931297.

When did GCA-7200A receive FDA 510(k) clearance?

GCA-7200A received FDA 510(k) clearance on 1993-07-27, under 510(k) number K931297.

Who is the listed applicant for GCA-7200A?

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 GCA-7200A?

The FDA product code for GCA-7200A is KPS.

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 SOFTWARE K131822ULTRAEXTEND USWS-900A V2.1 AND V3.1 K123097DOSE TRACKING SYSTEM MODEL XIDF-DTS801 K122613VANTAGE TITAN WITH HELIOS GRADIENT MODEL MRT-1504/US K121076ULTRAEXTEND FX, ULTRASOUND WORKSTATION PACKAGE K122842RADREX-I, SW V4.00 MODEL DRAD-3000E

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Related Devices (Code: KPS)

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.