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FDA 510(k)

ANGIOREX CAS-05A

K-Number: K941177 · 1994-06-06

ApplicantToshiba America Medical Systems, In.C
Decision Date1994-06-06
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ANGIOREX CAS-05A 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 1994-06-06 under 510(k) number K941177. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOREX CAS-05A?

ANGIOREX CAS-05A is a medical device that received FDA 510(k) clearance on 1994-06-06. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K941177.

When did ANGIOREX CAS-05A receive FDA 510(k) clearance?

ANGIOREX CAS-05A received FDA 510(k) clearance on 1994-06-06, under 510(k) number K941177.

Who is the listed applicant for ANGIOREX CAS-05A?

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 ANGIOREX CAS-05A?

The FDA product code for ANGIOREX CAS-05A is IZI.

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Related Devices (Code: IZI)

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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.

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