FDA 510(k), K203343, Wesper Lab

FDA 510(k), K203343, Wesper Lab

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510(K) Number: K203343
Device Name: Wesper Lab
Manufacturer: Wesper Inc.
Device Classification Name: Ventilatory Effort Recorder
Regulation Number: 868.2375
Classification Product Code: MNR
Date Received: 11/13/2020
Decision Date: 12/21/2021
Regulation Medical Specialty: Anesthesiology

Total Pages: 2,524
Fully Redacted Pages: 2,171
Content Pages: 353
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