FDA 510(k)

LEGIONELLA MWY SELECTIVE SUPPLEMENT

K-Number: K840331 · 1984-05-11

Decision Date1984-05-11

Product CodeJSK

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

LEGIONELLA MWY SELECTIVE SUPPLEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Oxoid U.S.A., Inc.. It received FDA 510(k) clearance on 1984-05-11 under 510(k) number K840331. The device is classified under product code JSK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEGIONELLA MWY SELECTIVE SUPPLEMENT?

LEGIONELLA MWY SELECTIVE SUPPLEMENT is a medical device that received FDA 510(k) clearance on 1984-05-11. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K840331.

When did LEGIONELLA MWY SELECTIVE SUPPLEMENT receive FDA 510(k) clearance?

LEGIONELLA MWY SELECTIVE SUPPLEMENT received FDA 510(k) clearance on 1984-05-11, under 510(k) number K840331.

Who is the listed applicant for LEGIONELLA MWY SELECTIVE SUPPLEMENT?

The FDA 510(k) record lists Oxoid U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEGIONELLA MWY SELECTIVE SUPPLEMENT?

The FDA product code for LEGIONELLA MWY SELECTIVE SUPPLEMENT is JSK.

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Other records listing Oxoid U.S.A., Inc. as applicant

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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.