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FDA 510(k)

MOVABLE CORE GUIDEWIRE

K-Number: K902152 · 1990-07-31

ApplicantGuidewire Technologies, Inc.
Decision Date1990-07-31
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MOVABLE CORE GUIDEWIRE is the device name listed in this FDA 510(k) record. The listed applicant is Guidewire Technologies, Inc.. It received FDA 510(k) clearance on 1990-07-31 under 510(k) number K902152. 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 MOVABLE CORE GUIDEWIRE?

MOVABLE CORE GUIDEWIRE is a medical device that received FDA 510(k) clearance on 1990-07-31. The listed applicant is Guidewire Technologies, Inc.. The 510(k) number is K902152.

When did MOVABLE CORE GUIDEWIRE receive FDA 510(k) clearance?

MOVABLE CORE GUIDEWIRE received FDA 510(k) clearance on 1990-07-31, under 510(k) number K902152.

Who is the listed applicant for MOVABLE CORE GUIDEWIRE?

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

What is the FDA product code for MOVABLE CORE GUIDEWIRE?

The FDA product code for MOVABLE CORE GUIDEWIRE is DQX.

Related Clinical Trials

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.

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Other records listing Guidewire Technologies, 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.

K902153TEFLON COATED GUIDEWIREK890959GUIDEWIRE

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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