InSee— 510(k) K241152
Substantially EquivalentTidal Medical Technologies, LLC
FDA 510(k) clearance K241152 for InSee, Substantially Equivalent on 2025-08-21. Applicant: Tidal Medical Technologies, LLC. Device class: 2.
Clearance details
- Applicant
- Tidal Medical Technologies, LLC
- Product code
- Code BWF
- Device class
- Class 2
- Regulation
- 21 CFR 868.5690
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Francisco, CA, US
Recent devices under product code BWF
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