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FDA 510(k)

MAXI TEST

K-Number: K904016 · 1990-10-15

ApplicantBhc Biotech , Ltd.
Decision Date1990-10-15
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAXI TEST is the device name listed in this FDA 510(k) record. The listed applicant is Bhc Biotech , Ltd.. It received FDA 510(k) clearance on 1990-10-15 under 510(k) number K904016. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAXI TEST?

MAXI TEST is a medical device that received FDA 510(k) clearance on 1990-10-15. The listed applicant is Bhc Biotech , Ltd.. The 510(k) number is K904016.

When did MAXI TEST receive FDA 510(k) clearance?

MAXI TEST received FDA 510(k) clearance on 1990-10-15, under 510(k) number K904016.

Who is the listed applicant for MAXI TEST?

The FDA 510(k) record lists Bhc Biotech , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAXI TEST?

The FDA product code for MAXI TEST is JHI.

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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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