FDA 510(k)

KEY CHAIN EMERGENCY AIRWAY

K-Number: K962312 · 1997-06-17

ApplicantFfrench Pocket Emergency Airway, Inc.

Decision Date1997-06-17

Product CodeBWC

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

KEY CHAIN EMERGENCY AIRWAY is the device name listed in this FDA 510(k) record. The listed applicant is Ffrench Pocket Emergency Airway, Inc.. It received FDA 510(k) clearance on 1997-06-17 under 510(k) number K962312. 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 KEY CHAIN EMERGENCY AIRWAY?

KEY CHAIN EMERGENCY AIRWAY is a medical device that received FDA 510(k) clearance on 1997-06-17. The listed applicant is Ffrench Pocket Emergency Airway, Inc.. The 510(k) number is K962312.

When did KEY CHAIN EMERGENCY AIRWAY receive FDA 510(k) clearance?

KEY CHAIN EMERGENCY AIRWAY received FDA 510(k) clearance on 1997-06-17, under 510(k) number K962312.

Who is the listed applicant for KEY CHAIN EMERGENCY AIRWAY?

The FDA 510(k) record lists Ffrench Pocket Emergency Airway, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KEY CHAIN EMERGENCY AIRWAY?

The FDA product code for KEY CHAIN EMERGENCY AIRWAY is BWC.

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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.