510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K141353Substantially Equivalent

Hudson Rci Aquapak Humidifier Adaptor

Teleflexmedical, Inc., Research Triangle Park NC / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K141353 is the FDA 510(k) clearance record for HUDSON RCI AQUAPAK HUMIDIFIER ADAPTOR, a class II device, cleared for Teleflexmedical, Inc. on under FDA product code BTT (Humidifier, Respiratory Gas, (Direct Patient Interface)). FDA records list 64 510(k) clearances for Teleflexmedical, Inc., from to . As of , FDA records show no recalls naming K141353.

Clearance record

Decision date
Received
(70 days to decision)
Product code
BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
Regulation
21 CFR 868.5450
Device class
Class II
Review panel
Anesthesiology
Applicant
Teleflexmedical, Inc. 2917 Week Dr., Research Triangle Park NC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code BTT

Trailing 12 months
5 clearances under product code BTT in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code BTT, trailing twelve months
MonthClearances
November 20250
December 20251
January 20262
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260