FDA 510(k)

SSA-380A

K-Number: K933743 · 1994-10-20

ApplicantToshiba America Medical Systems, In.C

Decision Date1994-10-20

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SSA-380A 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 1994-10-20 under 510(k) number K933743. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SSA-380A?

SSA-380A is a medical device that received FDA 510(k) clearance on 1994-10-20. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K933743.

When did SSA-380A receive FDA 510(k) clearance?

SSA-380A received FDA 510(k) clearance on 1994-10-20, under 510(k) number K933743.

Who is the listed applicant for SSA-380A?

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 SSA-380A?

The FDA product code for SSA-380A is IYN.

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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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.