FDA 510(k)

RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM

K-Number: K862909 · 1986-09-09

Decision Date1986-09-09

Product CodeBTO

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Medical Devices , Ltd.. It received FDA 510(k) clearance on 1986-09-09 under 510(k) number K862909. The device is classified under product code BTO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM?

RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM is a medical device that received FDA 510(k) clearance on 1986-09-09. The listed applicant is Intl. Medical Devices , Ltd.. The 510(k) number is K862909.

When did RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM receive FDA 510(k) clearance?

RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM received FDA 510(k) clearance on 1986-09-09, under 510(k) number K862909.

Who is the listed applicant for RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM?

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

What is the FDA product code for RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM?

The FDA product code for RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM is BTO.

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Other records listing Intl. Medical Devices , Ltd. as applicant

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Related Devices (Code: BTO)

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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.