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FDA 510(k)

SUPER SHEATH XL INTRODUCER SHEATH

K-Number: K060190 · 2006-04-04

ApplicantTogo Medikit Co., Ltd.
Decision Date2006-04-04
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SUPER SHEATH XL INTRODUCER SHEATH is the device name listed in this FDA 510(k) record. The listed applicant is Togo Medikit Co., Ltd.. It received FDA 510(k) clearance on 2006-04-04 under 510(k) number K060190. 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 SUPER SHEATH XL INTRODUCER SHEATH?

SUPER SHEATH XL INTRODUCER SHEATH is a medical device that received FDA 510(k) clearance on 2006-04-04. The listed applicant is Togo Medikit Co., Ltd.. The 510(k) number is K060190.

When did SUPER SHEATH XL INTRODUCER SHEATH receive FDA 510(k) clearance?

SUPER SHEATH XL INTRODUCER SHEATH received FDA 510(k) clearance on 2006-04-04, under 510(k) number K060190.

Who is the listed applicant for SUPER SHEATH XL INTRODUCER SHEATH?

The FDA 510(k) record lists Togo Medikit Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPER SHEATH XL INTRODUCER SHEATH?

The FDA product code for SUPER SHEATH XL INTRODUCER SHEATH is DYB.

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Other records listing Togo Medikit Co., Ltd. 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.

K241230Super Sheath Introducer Sheath S-3N5/1005 S-3N7/1006 S-3W5/1007 S-3W7/1008K200379Super SheathK190001Supercath 5K172496SUPERCATH 5 (26G)K160592SUPERCATH 6K121504SUPER SHEATH INTRODUCER SHEATH AND SUPER SHEATH INTRODUCER SHEATH SETS

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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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