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FDA 510(k)

MODIFIED CASS SYSTEM

K-Number: K902488 · 1990-12-07

Decision Date1990-12-07
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODIFIED CASS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Instrumentation & Diagnostics Corp.(Midco). It received FDA 510(k) clearance on 1990-12-07 under 510(k) number K902488. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED CASS SYSTEM?

MODIFIED CASS SYSTEM is a medical device that received FDA 510(k) clearance on 1990-12-07. The listed applicant is Medical Instrumentation & Diagnostics Corp.(Midco). The 510(k) number is K902488.

When did MODIFIED CASS SYSTEM receive FDA 510(k) clearance?

MODIFIED CASS SYSTEM received FDA 510(k) clearance on 1990-12-07, under 510(k) number K902488.

Who is the listed applicant for MODIFIED CASS SYSTEM?

The FDA 510(k) record lists Medical Instrumentation & Diagnostics Corp.(Midco) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED CASS SYSTEM?

The FDA product code for MODIFIED CASS SYSTEM is KXK.

Related Clinical Trials

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.

Other records listing Medical Instrumentation & Diagnostics Corp.(Midco) 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: KXK)

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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