FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HVT 2.0

K Number: K254078 · Decision Apr 13, 2026
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
220
Applicant Total
13
Review Days
116

Basic Information

Device Name
HVT 2.0
K Number
K254078
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5450
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vapotherm, Inc.
Date Received
December 18, 2025
Decision Date
April 13, 2026
Product Code
BTT
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BTT Humidifier, Respiratory Gas, (Direct Patient Interface)

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DEN170001 Precision Flow® HVNI
K111640 PRECISION FLOW(R) - HELIOX
K103316 FLOWREST
K072845 PRECISION FLOW
K070056 VAPOTHERM MODEL# 2000I AND 2000H
K042245 VAPOTHERM MODEL#2000I, 200H
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