SYSTAMATE ASPARTATE AMINOTRANSFERASE TEST TECHNICO
K-Number: K922857 · 1992-09-09
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Device Summary
Frequently Asked Questions
What is the SYSTAMATE ASPARTATE AMINOTRANSFERASE TEST TECHNICO?
SYSTAMATE ASPARTATE AMINOTRANSFERASE TEST TECHNICO is a medical device that received FDA 510(k) clearance on 1992-09-09. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K922857.
When did SYSTAMATE ASPARTATE AMINOTRANSFERASE TEST TECHNICO receive FDA 510(k) clearance?
SYSTAMATE ASPARTATE AMINOTRANSFERASE TEST TECHNICO received FDA 510(k) clearance on 1992-09-09, under 510(k) number K922857.
Who is the listed applicant for SYSTAMATE ASPARTATE AMINOTRANSFERASE TEST TECHNICO?
The FDA 510(k) record lists Em Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYSTAMATE ASPARTATE AMINOTRANSFERASE TEST TECHNICO?
The FDA product code for SYSTAMATE ASPARTATE AMINOTRANSFERASE TEST TECHNICO is CIT.
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 Em Diagnostic Systems, Inc. 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: CIT)
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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