FDA 510(k) Applications Submitted by Vapotherm, Inc.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K111640 |
06/13/2011 |
PRECISION FLOW(R) - HELIOX |
VAPOTHERM, INC. |
| K103316 |
11/10/2010 |
FLOWREST |
VAPOTHERM, INC. |
| K070056 |
01/05/2007 |
VAPOTHERM MODEL# 2000I AND 2000H |
VAPOTHERM, INC. |
| K072845 |
10/04/2007 |
PRECISION FLOW |
VAPOTHERM, INC. |
| K042245 |
08/19/2004 |
VAPOTHERM MODEL#2000I, 200H |
VAPOTHERM, INC. |
| K013486 |
10/19/2001 |
VAPOTHERM 2000H |
VAPOTHERM, INC. |
| K191010 |
04/16/2019 |
Palladium High Flow Therapy System |
Vapotherm, Inc. |
| DEN170001 |
01/03/2017 |
Precision Flow« HVNI |
VAPOTHERM, INC. |
| K000401 |
02/07/2000 |
VAPOTHERM, MODEL 2000I |
VAPOTHERM, INC. |
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