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FDA 510(k)

TRIMED PLAN, VERSION 2.2

K-Number: K031088 · 2004-07-23

ApplicantTrimed Systems, Inc.
Decision Date2004-07-23
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TRIMED PLAN, VERSION 2.2 is the device name listed in this FDA 510(k) record. The listed applicant is Trimed Systems, Inc.. It received FDA 510(k) clearance on 2004-07-23 under 510(k) number K031088. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIMED PLAN, VERSION 2.2?

TRIMED PLAN, VERSION 2.2 is a medical device that received FDA 510(k) clearance on 2004-07-23. The listed applicant is Trimed Systems, Inc.. The 510(k) number is K031088.

When did TRIMED PLAN, VERSION 2.2 receive FDA 510(k) clearance?

TRIMED PLAN, VERSION 2.2 received FDA 510(k) clearance on 2004-07-23, under 510(k) number K031088.

Who is the listed applicant for TRIMED PLAN, VERSION 2.2?

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

What is the FDA product code for TRIMED PLAN, VERSION 2.2?

The FDA product code for TRIMED PLAN, VERSION 2.2 is MUJ.

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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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