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FDA 510(k)

INRA MENEZO B2 MEDIA

K-Number: K844288 · 1984-12-13

Decision Date1984-12-13
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

INRA MENEZO B2 MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is Fcs Laboratories, Inc.. It received FDA 510(k) clearance on 1984-12-13 under 510(k) number K844288. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INRA MENEZO B2 MEDIA?

INRA MENEZO B2 MEDIA is a medical device that received FDA 510(k) clearance on 1984-12-13. The listed applicant is Fcs Laboratories, Inc.. The 510(k) number is K844288.

When did INRA MENEZO B2 MEDIA receive FDA 510(k) clearance?

INRA MENEZO B2 MEDIA received FDA 510(k) clearance on 1984-12-13, under 510(k) number K844288.

Who is the listed applicant for INRA MENEZO B2 MEDIA?

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

What is the FDA product code for INRA MENEZO B2 MEDIA?

The FDA product code for INRA MENEZO B2 MEDIA is KIT.

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.

Related Devices (Code: KIT)

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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