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FDA 510(k)

CORITAXIC MULTI-MODAL STEREOTAXI WORKSTATION

K-Number: K915791 · 1992-07-10

ApplicantCoritechs, Inc.
Decision Date1992-07-10
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CORITAXIC MULTI-MODAL STEREOTAXI WORKSTATION is the device name listed in this FDA 510(k) record. The listed applicant is Coritechs, Inc.. It received FDA 510(k) clearance on 1992-07-10 under 510(k) number K915791. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORITAXIC MULTI-MODAL STEREOTAXI WORKSTATION?

CORITAXIC MULTI-MODAL STEREOTAXI WORKSTATION is a medical device that received FDA 510(k) clearance on 1992-07-10. The listed applicant is Coritechs, Inc.. The 510(k) number is K915791.

When did CORITAXIC MULTI-MODAL STEREOTAXI WORKSTATION receive FDA 510(k) clearance?

CORITAXIC MULTI-MODAL STEREOTAXI WORKSTATION received FDA 510(k) clearance on 1992-07-10, under 510(k) number K915791.

Who is the listed applicant for CORITAXIC MULTI-MODAL STEREOTAXI WORKSTATION?

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

What is the FDA product code for CORITAXIC MULTI-MODAL STEREOTAXI WORKSTATION?

The FDA product code for CORITAXIC MULTI-MODAL STEREOTAXI WORKSTATION is HAW.

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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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