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FDA 510(k)

INTRODUCER SHEATH, VESSEL DILATOR

K-Number: K992309 · 1999-10-07

ApplicantBoston Scientific Corp
Decision Date1999-10-07
Product CodeDYB
Advisory CommitteeCV
DecisionUnknown

Device Summary

INTRODUCER SHEATH, VESSEL DILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 1999-10-07 under 510(k) number K992309. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the INTRODUCER SHEATH, VESSEL DILATOR?

INTRODUCER SHEATH, VESSEL DILATOR is a medical device that received FDA 510(k) clearance on 1999-10-07. The listed applicant is Boston Scientific Corp. The 510(k) number is K992309.

When did INTRODUCER SHEATH, VESSEL DILATOR receive FDA 510(k) clearance?

INTRODUCER SHEATH, VESSEL DILATOR received FDA 510(k) clearance on 1999-10-07, under 510(k) number K992309.

Who is the listed applicant for INTRODUCER SHEATH, VESSEL DILATOR?

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

What is the FDA product code for INTRODUCER SHEATH, VESSEL DILATOR?

The FDA product code for INTRODUCER SHEATH, VESSEL DILATOR is DYB.

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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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