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FDA 510(k)

CT Midline

K-Number: K170770 · 2017-07-25

ApplicantMedical Components, Inc. (dba MedComp)
Decision Date2017-07-25
Product CodePND
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CT Midline is a medical device manufactured by Medical Components, Inc. (dba MedComp). It received FDA 510(k) clearance on 2017-07-25 under approval number K170770. The device is classified under product code PND. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CT Midline?

CT Midline is a medical device that received FDA 510(k) clearance on 2017-07-25. It is manufactured by Medical Components, Inc. (dba MedComp). The 510(k) number is K170770.

When was CT Midline approved by the FDA?

CT Midline received FDA 510(k) clearance on 2017-07-25, under approval number K170770.

What company makes CT Midline?

CT Midline is manufactured by Medical Components, Inc. (dba MedComp).

What is the FDA product code for CT Midline?

The FDA product code for CT Midline is PND.

Other Devices by Medical Components, Inc. (dba MedComp)

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Related Devices (Code: PND)

K162900PowerMidline CatheterC.R. Bard, Inc. K161313ARROW Pressure Injectable Midline Catheter with Chlorag+ard Antimicrobial and Antithrombogenic TechnologyArrow International, Inc. (Subsidiary of Teleflex, Inc.) K153393PowerMidline CatheterC.R. Bard, Inc. K171483ArchFlo CT MidlineMedcomp (Dba Medical Components, Inc.) K170158PowerGlide ST Midline CatheterC.R. Bard, Inc. K181208Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL CatheterVygon USA

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.

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