510(k) K241152

Device
InSee
Applicant
Tidal Medical Technologies, LLC
510(k) number
K241152
Product code
BWF
Decision
Substantially Equivalent (SESE)
Decision date
2025-08-21
Date received
2024-04-26
Regulation
868.5690
Classification name
Spirometer, Therapeutic (Incentive)
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Mehdi Arani
Address
44 Montgomery St. Suite 2-155 San Francisco CA US 94101 94101

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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