FDA 510(k)

IVT 0.014 GUIDE WIRE

K-Number: K895903 · 1990-01-04

Decision Date1990-01-04

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

IVT 0.014 GUIDE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Intensive Technology, Inc.. It received FDA 510(k) clearance on 1990-01-04 under 510(k) number K895903. 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 IVT 0.014 GUIDE WIRE?

IVT 0.014 GUIDE WIRE is a medical device that received FDA 510(k) clearance on 1990-01-04. The listed applicant is Intensive Technology, Inc.. The 510(k) number is K895903.

When did IVT 0.014 GUIDE WIRE receive FDA 510(k) clearance?

IVT 0.014 GUIDE WIRE received FDA 510(k) clearance on 1990-01-04, under 510(k) number K895903.

Who is the listed applicant for IVT 0.014 GUIDE WIRE?

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

What is the FDA product code for IVT 0.014 GUIDE WIRE?

The FDA product code for IVT 0.014 GUIDE WIRE is DQX.

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Other records listing Intensive Technology, Inc. as applicant

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Related Devices (Code: DQX)

K253146Hyperdrive 35 GuidewireRapid-Medical , Ltd.K261281CROSSLEAD Standard 035 and CROSSLEAD Stiff 035Filmecc Co., Ltd.K253667Accoat Guide WireSp Medical A/S K261640Merit 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.