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FDA 510(k)

CORDIS CATHETER SHEATH INTRODUCERS,STERI-SLEEVES

K-Number: K855126 · 1986-02-26

ApplicantCordis Corp.
Decision Date1986-02-26
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CORDIS CATHETER SHEATH INTRODUCERS,STERI-SLEEVES is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1986-02-26 under 510(k) number K855126. 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 CORDIS CATHETER SHEATH INTRODUCERS,STERI-SLEEVES?

CORDIS CATHETER SHEATH INTRODUCERS,STERI-SLEEVES is a medical device that received FDA 510(k) clearance on 1986-02-26. The listed applicant is Cordis Corp.. The 510(k) number is K855126.

When did CORDIS CATHETER SHEATH INTRODUCERS,STERI-SLEEVES receive FDA 510(k) clearance?

CORDIS CATHETER SHEATH INTRODUCERS,STERI-SLEEVES received FDA 510(k) clearance on 1986-02-26, under 510(k) number K855126.

Who is the listed applicant for CORDIS CATHETER SHEATH INTRODUCERS,STERI-SLEEVES?

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

What is the FDA product code for CORDIS CATHETER SHEATH INTRODUCERS,STERI-SLEEVES?

The FDA product code for CORDIS CATHETER SHEATH INTRODUCERS,STERI-SLEEVES is DYB.

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Other records listing Cordis Corp. 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.

K112797POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETERK101651ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIREK082143MICRO GUIDE CATHETER XPK062798SMART NITINOL SELF-EXPANDING STENT, MODEL C06120MB, C07120MB, C08120MB, C06150MB, C07150MB, C08150MBK060877PALMAZ BLUE .014 TRANSHEPATIC BILIARY STENT SYSTEM-MODEL PB1550,BAS,BAX,PB1560,BAS,BAX,PB1850,BAS,BAXPB1860BAS,BAXK050645CORDIS AMIIA .014 PTA BALLOON CATHETER

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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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