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FDA 510(k)

GUIDE WIRE BOWL

K-Number: K873942 · 1987-12-23

ApplicantCondor Medical
Decision Date1987-12-23
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GUIDE WIRE BOWL is the device name listed in this FDA 510(k) record. The listed applicant is Condor Medical. It received FDA 510(k) clearance on 1987-12-23 under 510(k) number K873942. 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 GUIDE WIRE BOWL?

GUIDE WIRE BOWL is a medical device that received FDA 510(k) clearance on 1987-12-23. The listed applicant is Condor Medical. The 510(k) number is K873942.

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

GUIDE WIRE BOWL received FDA 510(k) clearance on 1987-12-23, under 510(k) number K873942.

Who is the listed applicant for GUIDE WIRE BOWL?

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

What is the FDA product code for GUIDE WIRE BOWL?

The FDA product code for GUIDE WIRE BOWL 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 Condor Medical 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.

K873985FLUORO COVERK8737093 RING ATTACHMENT FOR SYRINGES

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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