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FDA 510(k)

0.016 GUIDE WIRE FOR NEUROLOGICAL ENDOSCOPE

K-Number: K913074 · 1991-11-05

ApplicantTerumo Medical Corp.
Decision Date1991-11-05
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

0.016 GUIDE WIRE FOR NEUROLOGICAL ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corp.. It received FDA 510(k) clearance on 1991-11-05 under 510(k) number K913074. 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 0.016 GUIDE WIRE FOR NEUROLOGICAL ENDOSCOPE?

0.016 GUIDE WIRE FOR NEUROLOGICAL ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1991-11-05. The listed applicant is Terumo Medical Corp.. The 510(k) number is K913074.

When did 0.016 GUIDE WIRE FOR NEUROLOGICAL ENDOSCOPE receive FDA 510(k) clearance?

0.016 GUIDE WIRE FOR NEUROLOGICAL ENDOSCOPE received FDA 510(k) clearance on 1991-11-05, under 510(k) number K913074.

Who is the listed applicant for 0.016 GUIDE WIRE FOR NEUROLOGICAL ENDOSCOPE?

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

What is the FDA product code for 0.016 GUIDE WIRE FOR NEUROLOGICAL ENDOSCOPE?

The FDA product code for 0.016 GUIDE WIRE FOR NEUROLOGICAL ENDOSCOPE is DQX.

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Other records listing Terumo Medical Corp. 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.

K111606PINNACLE PRECISION ACCESS SYSTEMK111556GLIDECROSS SUPPORT CATHETERK110540TERUMO SUPPORT CATHETERK102008GLIDESHEATHK091329PINNACLE DESTINATION PERIPHERAL GUIDING SHEATHK082997TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER

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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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