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FDA 510(k)

TARGET THERAPEUTICS SEEKER-16 STEERABLE GUIDEWIRE

K-Number: K884198 · 1988-12-13

ApplicantTarget Therapeutics
Decision Date1988-12-13
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TARGET THERAPEUTICS SEEKER-16 STEERABLE GUIDEWIRE is the device name listed in this FDA 510(k) record. The listed applicant is Target Therapeutics. It received FDA 510(k) clearance on 1988-12-13 under 510(k) number K884198. 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 TARGET THERAPEUTICS SEEKER-16 STEERABLE GUIDEWIRE?

TARGET THERAPEUTICS SEEKER-16 STEERABLE GUIDEWIRE is a medical device that received FDA 510(k) clearance on 1988-12-13. The listed applicant is Target Therapeutics. The 510(k) number is K884198.

When did TARGET THERAPEUTICS SEEKER-16 STEERABLE GUIDEWIRE receive FDA 510(k) clearance?

TARGET THERAPEUTICS SEEKER-16 STEERABLE GUIDEWIRE received FDA 510(k) clearance on 1988-12-13, under 510(k) number K884198.

Who is the listed applicant for TARGET THERAPEUTICS SEEKER-16 STEERABLE GUIDEWIRE?

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

What is the FDA product code for TARGET THERAPEUTICS SEEKER-16 STEERABLE GUIDEWIRE?

The FDA product code for TARGET THERAPEUTICS SEEKER-16 STEERABLE GUIDEWIRE is DQX.

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Other records listing Target Therapeutics 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.

K965071DETACHABLE SLICONE BALLOON (DSB)K964488DETACHABLE SILICONE BALLOON (DSB)K964210RETRIEVER IIK971395GUGLIELMI DETACHABLE COIL (GDC), FIBERED PLATINUM COIL, .035 TYPE, BERENSTEIN LIQUID COIL, FIBERED PLATINUM COILS, ACCEK965189SPINNAKERK964112BERENSTEIN COIL

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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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