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FDA 510(k)

GUIDEWIRE, MODEL G-V220-3527S AND OTHERS

K-Number: K072354 · 2007-12-07

ApplicantAccellent, Inc.
Decision Date2007-12-07
Product CodeOCY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GUIDEWIRE, MODEL G-V220-3527S AND OTHERS is the device name listed in this FDA 510(k) record. The listed applicant is Accellent, Inc.. It received FDA 510(k) clearance on 2007-12-07 under 510(k) number K072354. The device is classified under product code OCY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GUIDEWIRE, MODEL G-V220-3527S AND OTHERS?

GUIDEWIRE, MODEL G-V220-3527S AND OTHERS is a medical device that received FDA 510(k) clearance on 2007-12-07. The listed applicant is Accellent, Inc.. The 510(k) number is K072354.

When did GUIDEWIRE, MODEL G-V220-3527S AND OTHERS receive FDA 510(k) clearance?

GUIDEWIRE, MODEL G-V220-3527S AND OTHERS received FDA 510(k) clearance on 2007-12-07, under 510(k) number K072354.

Who is the listed applicant for GUIDEWIRE, MODEL G-V220-3527S AND OTHERS?

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

What is the FDA product code for GUIDEWIRE, MODEL G-V220-3527S AND OTHERS?

The FDA product code for GUIDEWIRE, MODEL G-V220-3527S AND OTHERS is OCY.

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Related Devices (Code: OCY)

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.

K153264EasyPass GuidewireMedi-Globe CorporationK131072ORCHESTRA HYDROPHILIC GUIDEWIRE STANDARD ANGLED, ORCHESTRA HYDROPHILIC GUIDEWIRE STRAIGHT STIFF, ORCHESTRA HYDROPHILICColoplast A/SK124052OSTAVI HYDROPHILIC GUIDEWIRELake Region MedicalK123438XENX STONE MANAGEMENT DEVICEXenolith MedicalK123439NEO ERCP GUIDEWIRENeometrics, Inc.K122816AXCESS SOFT TIP WIRE GUIDEWilson-Cook Medical, 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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