FDA 510(k)

Nylon flexTAP(R)

Número K: K252374 · 2025-09-11

RequerenteAirway Technologies D/B/A Airway Management

Data da decisão2025-09-11

Código do produtoLRK

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Nylon flexTAP(R) is the device name listed in this FDA 510(k) record. The listed applicant is Airway Technologies D/B/A Airway Management. It received FDA 510(k) clearance on 2025-09-11 under 510(k) number K252374. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Nylon flexTAP(R)?

Nylon flexTAP(R) is a medical device that received FDA 510(k) clearance on 2025-09-11. The listed applicant is Airway Technologies D/B/A Airway Management. The 510(k) number is K252374.

When did Nylon flexTAP(R) receive FDA 510(k) clearance?

Nylon flexTAP(R) received FDA 510(k) clearance on 2025-09-11, under 510(k) number K252374.

Who is the listed applicant for Nylon flexTAP(R)?

The FDA 510(k) record lists Airway Technologies D/B/A Airway Management as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nylon flexTAP(R)?

The FDA product code for Nylon flexTAP(R) is LRK.

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