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FDA 510(k)

HYDROGLIDE SPRING GUIDE WIRES

K-Number: K841926 · 1985-01-02

ApplicantArgon Medical Corp.
Decision Date1985-01-02
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HYDROGLIDE SPRING GUIDE WIRES is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Corp.. It received FDA 510(k) clearance on 1985-01-02 under 510(k) number K841926. 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 HYDROGLIDE SPRING GUIDE WIRES?

HYDROGLIDE SPRING GUIDE WIRES is a medical device that received FDA 510(k) clearance on 1985-01-02. The listed applicant is Argon Medical Corp.. The 510(k) number is K841926.

When did HYDROGLIDE SPRING GUIDE WIRES receive FDA 510(k) clearance?

HYDROGLIDE SPRING GUIDE WIRES received FDA 510(k) clearance on 1985-01-02, under 510(k) number K841926.

Who is the listed applicant for HYDROGLIDE SPRING GUIDE WIRES?

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

What is the FDA product code for HYDROGLIDE SPRING GUIDE WIRES?

The FDA product code for HYDROGLIDE SPRING GUIDE WIRES is DQX.

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Other records listing Argon Medical Corp. as applicant

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K904994CLOSED SYSTEM FLUSH SETK895511CATHETER BALLOON DILATOR PRESSURE GAUGEK894157OBTURATORK891022INTRODUCER FOR PTCA GUIDING CATHETERSK884375TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETERK882221OVER THE NEEDLE CATHETER, ARTERIAL CATHETER NEEDLE

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Related Devices (Code: DQX)

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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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