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FDA 510(k)

PERCUTANEOUS CATHETER INTRODUCER KIT

K-Number: K903906 · 1990-09-26

ApplicantIntec Medical, Inc.
Decision Date1990-09-26
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS CATHETER INTRODUCER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Intec Medical, Inc.. It received FDA 510(k) clearance on 1990-09-26 under 510(k) number K903906. 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 PERCUTANEOUS CATHETER INTRODUCER KIT?

PERCUTANEOUS CATHETER INTRODUCER KIT is a medical device that received FDA 510(k) clearance on 1990-09-26. The listed applicant is Intec Medical, Inc.. The 510(k) number is K903906.

When did PERCUTANEOUS CATHETER INTRODUCER KIT receive FDA 510(k) clearance?

PERCUTANEOUS CATHETER INTRODUCER KIT received FDA 510(k) clearance on 1990-09-26, under 510(k) number K903906.

Who is the listed applicant for PERCUTANEOUS CATHETER INTRODUCER KIT?

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

What is the FDA product code for PERCUTANEOUS CATHETER INTRODUCER KIT?

The FDA product code for PERCUTANEOUS CATHETER INTRODUCER KIT is DYB.

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Other records listing Intec Medical, Inc. 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.

K911840INTERFLO MEDICAL MODEL PA3-H CCO/PAC CATHETERK903217TAPERED TIP THE GUIDER CORONARY GUIDING CATHETERK900710INTERFLO MEDICAL MODEL F-1 THERMODILUTION CATHETERK903216THE GUIDER CORONARY GUIDING CATHETERK903840GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSYK900998INTERVENTIONAL MEDICAL Y ADAPTER W/ADJUST. VALVE

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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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