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FDA 510(k)

RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SET

K-Number: K130405 · 2013-11-06

ApplicantTeleflex Medical
Decision Date2013-11-06
Product CodeBWC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SET is the device name listed in this FDA 510(k) record. The listed applicant is Teleflex Medical. It received FDA 510(k) clearance on 2013-11-06 under 510(k) number K130405. The device is classified under product code BWC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SET?

RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SET is a medical device that received FDA 510(k) clearance on 2013-11-06. The listed applicant is Teleflex Medical. The 510(k) number is K130405.

When did RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SET receive FDA 510(k) clearance?

RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SET received FDA 510(k) clearance on 2013-11-06, under 510(k) number K130405.

Who is the listed applicant for RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SET?

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

What is the FDA product code for RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SET?

The FDA product code for RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SET is BWC.

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Related Devices (Code: BWC)

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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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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