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FDA 510(k)

THE WUSCOPE SYSTEM

K-Number: K941319 · 1994-10-04

ApplicantAchi Corp.
Decision Date1994-10-04
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THE WUSCOPE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Achi Corp.. It received FDA 510(k) clearance on 1994-10-04 under 510(k) number K941319. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE WUSCOPE SYSTEM?

THE WUSCOPE SYSTEM is a medical device that received FDA 510(k) clearance on 1994-10-04. The listed applicant is Achi Corp.. The 510(k) number is K941319.

When did THE WUSCOPE SYSTEM receive FDA 510(k) clearance?

THE WUSCOPE SYSTEM received FDA 510(k) clearance on 1994-10-04, under 510(k) number K941319.

Who is the listed applicant for THE WUSCOPE SYSTEM?

The FDA 510(k) record lists Achi Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE WUSCOPE SYSTEM?

The FDA product code for THE WUSCOPE SYSTEM is CCW.

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Related Devices (Code: CCW)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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