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FDA 510(k)

VISION WIRE CORONARY GUIDEWIRE

K-Number: K082935 · 2008-12-04

ApplicantBiotronik, Inc.
Decision Date2008-12-04
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VISION WIRE CORONARY GUIDEWIRE is the device name listed in this FDA 510(k) record. The listed applicant is Biotronik, Inc.. It received FDA 510(k) clearance on 2008-12-04 under 510(k) number K082935. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISION WIRE CORONARY GUIDEWIRE?

VISION WIRE CORONARY GUIDEWIRE is a medical device that received FDA 510(k) clearance on 2008-12-04. The listed applicant is Biotronik, Inc.. The 510(k) number is K082935.

When did VISION WIRE CORONARY GUIDEWIRE receive FDA 510(k) clearance?

VISION WIRE CORONARY GUIDEWIRE received FDA 510(k) clearance on 2008-12-04, under 510(k) number K082935.

Who is the listed applicant for VISION WIRE CORONARY GUIDEWIRE?

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

What is the FDA product code for VISION WIRE CORONARY GUIDEWIRE?

The FDA product code for VISION WIRE CORONARY GUIDEWIRE is DQX.

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Related Devices (Code: DQX)

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.

K253146Hyperdrive 35 GuidewireRapid-Medical , Ltd.K261281CROSSLEAD Standard 035 and CROSSLEAD Stiff 035Filmecc Co., Ltd.K253667Accoat Guide WireSp Medical A/SK261640Merit MAK Nitinol/Gold-Tungsten Guide WireMerit Medical Ireland , Ltd.K254137InQwire Amplatz Guide WireMerit Medical Ireland, Ltd.K260544FMD Peripheral Guide Wire F-14 Flex 6; FMD Peripheral Guide Wire F-14 Tapered 40; FMD Peripheral Guide Wire F-18 Flex SP; FMD Peripheral Guide Wire F-18 DP 25; FMD Peripheral Guide Wire F-18 Tapered 40FMD Co., Ltd.

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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