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FDA 510(k)

CRIT-SCAN

K-Number: K910077 · 1992-06-02

Decision Date1992-06-02
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CRIT-SCAN is the device name listed in this FDA 510(k) record. The listed applicant is Noninvasive Medical Technology Corp.. It received FDA 510(k) clearance on 1992-06-02 under 510(k) number K910077. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRIT-SCAN?

CRIT-SCAN is a medical device that received FDA 510(k) clearance on 1992-06-02. The listed applicant is Noninvasive Medical Technology Corp.. The 510(k) number is K910077.

When did CRIT-SCAN receive FDA 510(k) clearance?

CRIT-SCAN received FDA 510(k) clearance on 1992-06-02, under 510(k) number K910077.

Who is the listed applicant for CRIT-SCAN?

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

What is the FDA product code for CRIT-SCAN?

The FDA product code for CRIT-SCAN is DQA.

Other records listing Noninvasive Medical Technology Corp. 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.

Related Devices (Code: DQA)

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.

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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