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FDA 510(k)

WEISS EMERGENCY AIRWAY SYSTEM

K-Number: K790650 · 1979-06-27

ApplicantIntl. Medical Devices , Ltd.
Decision Date1979-06-27
Product CodeBWC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

WEISS EMERGENCY AIRWAY 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 1979-06-27 under 510(k) number K790650. 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 WEISS EMERGENCY AIRWAY SYSTEM?

WEISS EMERGENCY AIRWAY SYSTEM is a medical device that received FDA 510(k) clearance on 1979-06-27. The listed applicant is Intl. Medical Devices , Ltd.. The 510(k) number is K790650.

When did WEISS EMERGENCY AIRWAY SYSTEM receive FDA 510(k) clearance?

WEISS EMERGENCY AIRWAY SYSTEM received FDA 510(k) clearance on 1979-06-27, under 510(k) number K790650.

Who is the listed applicant for WEISS EMERGENCY AIRWAY 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 WEISS EMERGENCY AIRWAY SYSTEM?

The FDA product code for WEISS EMERGENCY AIRWAY SYSTEM is BWC.

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Other records listing Intl. Medical Devices , Ltd. 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.

K913540PEDIA-THOR THORACOSTOMY KITK913541NEO-THOR THORACOSTOMY KITK913542THORACIC CATHETER WITH GUIDEK913539THORACIC CATHTER STYLETK913543THORACIC CATHETER STYLETK862909RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM

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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.

K200190ScalpelCricVBM Medizintechnik GmbHK160200Melker Cuffed Emergency Cricothyrotomy Catheter Sets, Melker Universal Cricothyrotomy Catheter SetCook IncorporatedK153761Emergency Transtracheal Airway CatheterCook IncorporatedK130405RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SETTeleflex MedicalK050166PORTEX EMERGENCY CRICOTHYROIDOTOMY KITSmiths MedicalK013252PATIL EMERGENCY CRICOTHYROTOMY CATHETER SETCook, Inc.

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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