Nylon flexTAP(R)
K-Number: K252374 · 2025-09-11
Decision Date2025-09-11
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Nylon flexTAP(R) is a medical device manufactured by Airway Technologies D/B/A Airway Management. It received FDA 510(k) clearance on 2025-09-11 under approval number K252374. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Nylon flexTAP(R)?
Nylon flexTAP(R) is a medical device that received FDA 510(k) clearance on 2025-09-11. It is manufactured by Airway Technologies D/B/A Airway Management. The 510(k) number is K252374.
When was Nylon flexTAP(R) approved by the FDA?
Nylon flexTAP(R) received FDA 510(k) clearance on 2025-09-11, under approval number K252374.
What company makes Nylon flexTAP(R)?
Nylon flexTAP(R) is manufactured by Airway Technologies D/B/A Airway Management.
What is the FDA product code for Nylon flexTAP(R)?
The FDA product code for Nylon flexTAP(R) is LRK.
Related Devices (Code: LRK)
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.