MODIFIED CASS SYSTEM
K-Number: K902488 · 1990-12-07
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Device Summary
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
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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