VAPOTHERM MODEL# 2000I AND 2000H— 510(k) K070056

Substantially Equivalent

Vapotherm, Inc.

FDA 510(k) clearance K070056 for VAPOTHERM MODEL# 2000I AND 2000H, Substantially Equivalent on 2007-04-13. Applicant: Vapotherm, Inc..

Clearance details

Applicant: Vapotherm, Inc.
Product code: Code BTT
Advisory panel: Anesthesiology
Date received: 2007-01-05
Decision date: 2007-04-13
Decision: Substantially Equivalent
Clearance type: Special
Location: Washington, DC, US

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Adverse events under product code BTT

product code BTT

Death: 60
Injury: 152
Malfunction: 7,232
Other: 2
Total: 7,446

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.