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FDA 510(k)

SOLOPATH RE-COLLAPSIBLE ACCESS SYSTEM

K-Number: K121404 · 2013-05-03

ApplicantOnset Medical Corporation
Decision Date2013-05-03
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SOLOPATH RE-COLLAPSIBLE ACCESS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Onset Medical Corporation. It received FDA 510(k) clearance on 2013-05-03 under 510(k) number K121404. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLOPATH RE-COLLAPSIBLE ACCESS SYSTEM?

SOLOPATH RE-COLLAPSIBLE ACCESS SYSTEM is a medical device that received FDA 510(k) clearance on 2013-05-03. The listed applicant is Onset Medical Corporation. The 510(k) number is K121404.

When did SOLOPATH RE-COLLAPSIBLE ACCESS SYSTEM receive FDA 510(k) clearance?

SOLOPATH RE-COLLAPSIBLE ACCESS SYSTEM received FDA 510(k) clearance on 2013-05-03, under 510(k) number K121404.

Who is the listed applicant for SOLOPATH RE-COLLAPSIBLE ACCESS SYSTEM?

The FDA 510(k) record lists Onset Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOLOPATH RE-COLLAPSIBLE ACCESS SYSTEM?

The FDA product code for SOLOPATH RE-COLLAPSIBLE ACCESS SYSTEM is DYB.

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Other records listing Onset Medical Corporation 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.

K152498SoloPath Re-Collapsible Access SystemK112629ONSET ACCESS CATHETER SYSTEMK100819THE SOLOPATH BALLOON EXPANDABLE TRANSFEMORAL INTRODUCERK092014SOLOPATH BALLOON EXPANDABLE TRANSFEMORAL INTRODUCERK062852BALLOON EXPANDABLE TRANSSEPTAL INDRODUCER, MODELS BETI-1840 AND BETI-1870K061009PATHWAY BALLOON EXPANDABLE URETERAL ACCESS SHEATH, MODEL BEUS

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Related Devices (Code: DYB)

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.

K253526NAMIC Dilator and SheathMedline Industries, LPK261529Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set/ Microintroducer Kit / Microintroducer Kit (SIS05C); Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set / Microintroducer Kit / Microintroducer Kit (IS01); Introducer Kit / Microintroducer Kit / Introducer Set /Microintroducer Set / Micro Introducer Sheath Set / Introducer Sheath Set (NIS04)Hartman Medical Group, LLCK261242SimplGuidePendracareK261950Health Line Tearaway IntroducerHealth Line International CorporationK261492FieldFlex Steerable SheathCenterPoint Systems, LLCK260606Echo Large Bore Introducer SheathEcho Medical, LLC

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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