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FDA 510(k)

SCIMED TRANSEND STEERABLE GUIDE WIRE AND ACCESSORIES

K-Number: K941710 · 1994-09-01

Decision Date1994-09-01
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SCIMED TRANSEND STEERABLE GUIDE WIRE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Scimed Peripheral Interventions. It received FDA 510(k) clearance on 1994-09-01 under 510(k) number K941710. 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 SCIMED TRANSEND STEERABLE GUIDE WIRE AND ACCESSORIES?

SCIMED TRANSEND STEERABLE GUIDE WIRE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1994-09-01. The listed applicant is Scimed Peripheral Interventions. The 510(k) number is K941710.

When did SCIMED TRANSEND STEERABLE GUIDE WIRE AND ACCESSORIES receive FDA 510(k) clearance?

SCIMED TRANSEND STEERABLE GUIDE WIRE AND ACCESSORIES received FDA 510(k) clearance on 1994-09-01, under 510(k) number K941710.

Who is the listed applicant for SCIMED TRANSEND STEERABLE GUIDE WIRE AND ACCESSORIES?

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

What is the FDA product code for SCIMED TRANSEND STEERABLE GUIDE WIRE AND ACCESSORIES?

The FDA product code for SCIMED TRANSEND STEERABLE GUIDE WIRE AND ACCESSORIES 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.

Other records listing Scimed Peripheral Interventions 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.

View all 8 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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