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FDA 510(k)

ALANINE AMINOTRANSFERASE (ALT) TEST

K-Number: K935180 · 1994-01-13

Decision Date1994-01-13
Product CodeCKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ALANINE AMINOTRANSFERASE (ALT) TEST is the device name listed in this FDA 510(k) record. The listed applicant is Em Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1994-01-13 under 510(k) number K935180. The device is classified under product code CKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALANINE AMINOTRANSFERASE (ALT) TEST?

ALANINE AMINOTRANSFERASE (ALT) TEST is a medical device that received FDA 510(k) clearance on 1994-01-13. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K935180.

When did ALANINE AMINOTRANSFERASE (ALT) TEST receive FDA 510(k) clearance?

ALANINE AMINOTRANSFERASE (ALT) TEST received FDA 510(k) clearance on 1994-01-13, under 510(k) number K935180.

Who is the listed applicant for ALANINE AMINOTRANSFERASE (ALT) TEST?

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 ALANINE AMINOTRANSFERASE (ALT) TEST?

The FDA product code for ALANINE AMINOTRANSFERASE (ALT) TEST is CKA.

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.

View all 288 devices →

Related Devices (Code: CKA)

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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