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FDA 510(k)

TRXF INTELLIGENT DOSING SYSTEM (IDS) -DOSING CALCULATOR SUITE

K-Number: K011571 · 2001-08-09

ApplicantThe RX Files Corp.
Decision Date2001-08-09
Product CodeNDC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRXF INTELLIGENT DOSING SYSTEM (IDS) -DOSING CALCULATOR SUITE is the device name listed in this FDA 510(k) record. The listed applicant is The RX Files Corp.. It received FDA 510(k) clearance on 2001-08-09 under 510(k) number K011571. The device is classified under product code NDC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRXF INTELLIGENT DOSING SYSTEM (IDS) -DOSING CALCULATOR SUITE?

TRXF INTELLIGENT DOSING SYSTEM (IDS) -DOSING CALCULATOR SUITE is a medical device that received FDA 510(k) clearance on 2001-08-09. The listed applicant is The RX Files Corp.. The 510(k) number is K011571.

When did TRXF INTELLIGENT DOSING SYSTEM (IDS) -DOSING CALCULATOR SUITE receive FDA 510(k) clearance?

TRXF INTELLIGENT DOSING SYSTEM (IDS) -DOSING CALCULATOR SUITE received FDA 510(k) clearance on 2001-08-09, under 510(k) number K011571.

Who is the listed applicant for TRXF INTELLIGENT DOSING SYSTEM (IDS) -DOSING CALCULATOR SUITE?

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

What is the FDA product code for TRXF INTELLIGENT DOSING SYSTEM (IDS) -DOSING CALCULATOR SUITE?

The FDA product code for TRXF INTELLIGENT DOSING SYSTEM (IDS) -DOSING CALCULATOR SUITE is NDC.

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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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