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

Vapotherm Aerosol Adapter AAA-2

K Number: K220869 · Decision Oct 28, 2022
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
13
Review Days
217

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Basic Information

Device Name
Vapotherm Aerosol Adapter AAA-2
K Number
K220869
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5630
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vapotherm, Inc.
Date Received
March 25, 2022
Decision Date
October 28, 2022
Product Code
CAF
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
CAF Nebulizer (Direct Patient Interface)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CAF), ordered by most recent decision date.

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Other Clearances by Vapotherm, Inc.

K Number Device Name
K254078 HVT 2.0
K221318 HVT 2.0
K203357 HVT 2.0
K191010 Palladium High Flow Therapy System
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
Search all 13 clearances from Vapotherm, Inc. →