FDA 510(k)

DRESSER ARGUS P/N 1818

K-Number: K905304 · 1991-04-17

Decision Date1991-04-17

Product CodeBTM

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

DRESSER ARGUS P/N 1818 is the device name listed in this FDA 510(k) record. The listed applicant is Dresser Argus, Inc.. It received FDA 510(k) clearance on 1991-04-17 under 510(k) number K905304. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRESSER ARGUS P/N 1818?

DRESSER ARGUS P/N 1818 is a medical device that received FDA 510(k) clearance on 1991-04-17. The listed applicant is Dresser Argus, Inc.. The 510(k) number is K905304.

When did DRESSER ARGUS P/N 1818 receive FDA 510(k) clearance?

DRESSER ARGUS P/N 1818 received FDA 510(k) clearance on 1991-04-17, under 510(k) number K905304.

Who is the listed applicant for DRESSER ARGUS P/N 1818?

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

What is the FDA product code for DRESSER ARGUS P/N 1818?

The FDA product code for DRESSER ARGUS P/N 1818 is BTM.

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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.