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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 the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc. (dba MedComp). It received FDA 510(k) clearance on 2017-07-25 under 510(k) 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. The listed applicant is Medical Components, Inc. (dba MedComp). The 510(k) number is K170770.

When did CT Midline receive FDA 510(k) clearance?

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

Who is the listed applicant for CT Midline?

The FDA 510(k) record lists Medical Components, Inc. (dba MedComp) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CT Midline?

The FDA product code for CT Midline is PND.

Other records listing Medical Components, Inc. (dba MedComp) as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: PND)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252402Midline CatheterTerumo Medical Products (Hangzhou) Co., Ltd.K213855Arrow Pressure Injectable Midline CatheterArrow International, LLC Subsidiary of Teleflex IncorporatedK213203Provena(TM) Midline CatheterC.R. Bard, Inc.K210047Stiletto Extended Dwell CatheterPiper Access, LLCK192802primeMidline CathetersPfm Medical, 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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