FDA 510(k)

INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM

K-Number: K002380 · 2000-09-05

Decision Date2000-09-05

Product CodeFRN

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 2000-09-05 under 510(k) number K002380. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM?

INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2000-09-05. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K002380.

When did INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM receive FDA 510(k) clearance?

INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM received FDA 510(k) clearance on 2000-09-05, under 510(k) number K002380.

Who is the listed applicant for INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM?

The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM?

The FDA product code for INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM is FRN.

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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.