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FDA 510(k)

CINEMAC QAS

K-Number: K936002 · 1994-09-09

ApplicantXre Corp.
Decision Date1994-09-09
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CINEMAC QAS is the device name listed in this FDA 510(k) record. The listed applicant is Xre Corp.. It received FDA 510(k) clearance on 1994-09-09 under 510(k) number K936002. 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 CINEMAC QAS?

CINEMAC QAS is a medical device that received FDA 510(k) clearance on 1994-09-09. The listed applicant is Xre Corp.. The 510(k) number is K936002.

When did CINEMAC QAS receive FDA 510(k) clearance?

CINEMAC QAS received FDA 510(k) clearance on 1994-09-09, under 510(k) number K936002.

Who is the listed applicant for CINEMAC QAS?

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

What is the FDA product code for CINEMAC QAS?

The FDA product code for CINEMAC QAS is IZI.

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Other records listing Xre Corp. as applicant

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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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