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FDA 510(k)

CARDIOIMMUNE CARDIAC MARKER CONTROL LEVELS 1,2, AND 3

K-Number: K992430 · 1999-08-30

Decision Date1999-08-30
Product CodeJJT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CARDIOIMMUNE CARDIAC MARKER CONTROL LEVELS 1,2, AND 3 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Analysis Systems, Inc.. It received FDA 510(k) clearance on 1999-08-30 under 510(k) number K992430. The device is classified under product code JJT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIOIMMUNE CARDIAC MARKER CONTROL LEVELS 1,2, AND 3?

CARDIOIMMUNE CARDIAC MARKER CONTROL LEVELS 1,2, AND 3 is a medical device that received FDA 510(k) clearance on 1999-08-30. The listed applicant is Medical Analysis Systems, Inc.. The 510(k) number is K992430.

When did CARDIOIMMUNE CARDIAC MARKER CONTROL LEVELS 1,2, AND 3 receive FDA 510(k) clearance?

CARDIOIMMUNE CARDIAC MARKER CONTROL LEVELS 1,2, AND 3 received FDA 510(k) clearance on 1999-08-30, under 510(k) number K992430.

Who is the listed applicant for CARDIOIMMUNE CARDIAC MARKER CONTROL LEVELS 1,2, AND 3?

The FDA 510(k) record lists Medical Analysis Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARDIOIMMUNE CARDIAC MARKER CONTROL LEVELS 1,2, AND 3?

The FDA product code for CARDIOIMMUNE CARDIAC MARKER CONTROL LEVELS 1,2, AND 3 is JJT.

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 Analysis 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 107 devices →

Related Devices (Code: JJT)

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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