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FDA 510(k)

MYCOLOGY AGAR W/ANTIBOTICS

K-Number: K851590 · 1985-04-30

Decision Date1985-04-30
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MYCOLOGY AGAR W/ANTIBOTICS is the device name listed in this FDA 510(k) record. The listed applicant is Preferred Micro-Media. It received FDA 510(k) clearance on 1985-04-30 under 510(k) number K851590. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYCOLOGY AGAR W/ANTIBOTICS?

MYCOLOGY AGAR W/ANTIBOTICS is a medical device that received FDA 510(k) clearance on 1985-04-30. The listed applicant is Preferred Micro-Media. The 510(k) number is K851590.

When did MYCOLOGY AGAR W/ANTIBOTICS receive FDA 510(k) clearance?

MYCOLOGY AGAR W/ANTIBOTICS received FDA 510(k) clearance on 1985-04-30, under 510(k) number K851590.

Who is the listed applicant for MYCOLOGY AGAR W/ANTIBOTICS?

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

What is the FDA product code for MYCOLOGY AGAR W/ANTIBOTICS?

The FDA product code for MYCOLOGY AGAR W/ANTIBOTICS is JSJ.

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 Preferred Micro-Media 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 28 devices →

Related Devices (Code: JSJ)

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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