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FDA 510(k)

YEAST IDENTIFICATION PANEL

K-Number: K860575 · 1986-05-13

Decision Date1986-05-13
Product CodeJXB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

YEAST IDENTIFICATION PANEL is the device name listed in this FDA 510(k) record. The listed applicant is American Micro Scan. It received FDA 510(k) clearance on 1986-05-13 under 510(k) number K860575. The device is classified under product code JXB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YEAST IDENTIFICATION PANEL?

YEAST IDENTIFICATION PANEL is a medical device that received FDA 510(k) clearance on 1986-05-13. The listed applicant is American Micro Scan. The 510(k) number is K860575.

When did YEAST IDENTIFICATION PANEL receive FDA 510(k) clearance?

YEAST IDENTIFICATION PANEL received FDA 510(k) clearance on 1986-05-13, under 510(k) number K860575.

Who is the listed applicant for YEAST IDENTIFICATION PANEL?

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

What is the FDA product code for YEAST IDENTIFICATION PANEL?

The FDA product code for YEAST IDENTIFICATION PANEL is JXB.

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 American Micro Scan 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 24 devices →

Related Devices (Code: JXB)

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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