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FDA 510(k)

BAXTER SENSOR CORONARY GUIDEWIRE

K-Number: K923240 · 1992-09-23

ApplicantBaxter Healthcare Corp
Decision Date1992-09-23
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BAXTER SENSOR CORONARY GUIDEWIRE is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1992-09-23 under 510(k) number K923240. 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 BAXTER SENSOR CORONARY GUIDEWIRE?

BAXTER SENSOR CORONARY GUIDEWIRE is a medical device that received FDA 510(k) clearance on 1992-09-23. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K923240.

When did BAXTER SENSOR CORONARY GUIDEWIRE receive FDA 510(k) clearance?

BAXTER SENSOR CORONARY GUIDEWIRE received FDA 510(k) clearance on 1992-09-23, under 510(k) number K923240.

Who is the listed applicant for BAXTER SENSOR CORONARY GUIDEWIRE?

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

What is the FDA product code for BAXTER SENSOR CORONARY GUIDEWIRE?

The FDA product code for BAXTER SENSOR 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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