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FDA 510(k)

ARCHITECT STAT TROPONIN-1; MYOGLOBIN

K-Number: K070640 · 2007-09-13

Decision Date2007-09-13
Product CodeMMI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ARCHITECT STAT TROPONIN-1; MYOGLOBIN is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Diagnostics. It received FDA 510(k) clearance on 2007-09-13 under 510(k) number K070640. The device is classified under product code MMI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARCHITECT STAT TROPONIN-1; MYOGLOBIN?

ARCHITECT STAT TROPONIN-1; MYOGLOBIN is a medical device that received FDA 510(k) clearance on 2007-09-13. The listed applicant is Fisher Diagnostics. The 510(k) number is K070640.

When did ARCHITECT STAT TROPONIN-1; MYOGLOBIN receive FDA 510(k) clearance?

ARCHITECT STAT TROPONIN-1; MYOGLOBIN received FDA 510(k) clearance on 2007-09-13, under 510(k) number K070640.

Who is the listed applicant for ARCHITECT STAT TROPONIN-1; MYOGLOBIN?

The FDA 510(k) record lists Fisher Diagnostics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARCHITECT STAT TROPONIN-1; MYOGLOBIN?

The FDA product code for ARCHITECT STAT TROPONIN-1; MYOGLOBIN is MMI.

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 Fisher Diagnostics 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 16 devices →

Related Devices (Code: MMI)

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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