BlineSlide— 510(k) K261679
Substantially EquivalentDeep Breathe, Inc.
FDA 510(k) clearance K261679 for BlineSlide, Substantially Equivalent on 2026-10-23. Applicant: Deep Breathe, Inc.. Device class: 2.
Clearance details
- Applicant
- Deep Breathe, Inc.
- Product code
- Product code POK
- Device class
- Class 2
- Regulation
- 21 CFR 892.2060
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- London, CA
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