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FDA 510(k)

INTRODUCER, PERCUTANEOUS -- MODIFICATION

K-Number: K924491 · 1992-11-18

ApplicantMedamicus, Inc.
Decision Date1992-11-18
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INTRODUCER, PERCUTANEOUS -- MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Medamicus, Inc.. It received FDA 510(k) clearance on 1992-11-18 under 510(k) number K924491. 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 INTRODUCER, PERCUTANEOUS -- MODIFICATION?

INTRODUCER, PERCUTANEOUS -- MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-11-18. The listed applicant is Medamicus, Inc.. The 510(k) number is K924491.

When did INTRODUCER, PERCUTANEOUS -- MODIFICATION receive FDA 510(k) clearance?

INTRODUCER, PERCUTANEOUS -- MODIFICATION received FDA 510(k) clearance on 1992-11-18, under 510(k) number K924491.

Who is the listed applicant for INTRODUCER, PERCUTANEOUS -- MODIFICATION?

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

What is the FDA product code for INTRODUCER, PERCUTANEOUS -- MODIFICATION?

The FDA product code for INTRODUCER, PERCUTANEOUS -- MODIFICATION is DYB.

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Other records listing Medamicus, 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.

K040150MODIFICATION TO MEDAMICUS FLOWGUARD PEELABLE INTRODUCERK030905MEDAMICUS FLOWGUARD PEELABLE INTRODUCERK022689MODIFICATION TO MEDAMICUS AXIA RSNK021004VALVED PEELABLE INTRODUCERK020563MEDAMICUS AXIA RSNK013120PERCUTANEOUS INTRODUCER SET, MODEL 042294 AND KIT MODEL 3550-18

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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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