BlineSlide— 510(k) K252007

Substantially Equivalent

Deep Breathe, Inc.

FDA 510(k) clearance K252007 for BlineSlide, Substantially Equivalent on 2025-10-06. Applicant: Deep Breathe, Inc.. Device class: 2.

Clearance details

Applicant: Deep Breathe, Inc.
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2025-06-27
Decision date: 2025-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: London, CA

Download summary PDF View on FDA.gov ↗

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