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FDA 510(k)

EZ PLUS RETRIEVAL SHEATH, MODEL 38899-150

K-Number: K051179 · 2005-06-08

ApplicantBoston Scientific Corp
Decision Date2005-06-08
Product CodeNFA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EZ PLUS RETRIEVAL SHEATH, MODEL 38899-150 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 2005-06-08 under 510(k) number K051179. The device is classified under product code NFA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ PLUS RETRIEVAL SHEATH, MODEL 38899-150?

EZ PLUS RETRIEVAL SHEATH, MODEL 38899-150 is a medical device that received FDA 510(k) clearance on 2005-06-08. The listed applicant is Boston Scientific Corp. The 510(k) number is K051179.

When did EZ PLUS RETRIEVAL SHEATH, MODEL 38899-150 receive FDA 510(k) clearance?

EZ PLUS RETRIEVAL SHEATH, MODEL 38899-150 received FDA 510(k) clearance on 2005-06-08, under 510(k) number K051179.

Who is the listed applicant for EZ PLUS RETRIEVAL SHEATH, MODEL 38899-150?

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 EZ PLUS RETRIEVAL SHEATH, MODEL 38899-150?

The FDA product code for EZ PLUS RETRIEVAL SHEATH, MODEL 38899-150 is NFA.

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Related Devices (Code: NFA)

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.

K073523INTERCEPTOR PLUS CORONARY FILTER SYSTEMSMedtronic, Inc.K073563MODIFICATION TO PROXIS SYSTEMSt Jude MedicalK063785SPIDERFX EMBOLIC PROTECTION DEVICEEv3, Inc.K062870TRIACTIV FX EMBOLIC PROTECTION SYSTEM, MODEL PN 60040-02; -03Kensey Nash Corp.K060651PROXIS SYSTEM, MODEL EPS101St Jude MedicalK052523PROXIS SYSTEMVelocimed, Inc.

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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