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FDA 510(k)

BlineSlide

K-Number: K252007 · 2025-10-06

ApplicantDeep Breathe, Inc.
Decision Date2025-10-06
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BlineSlide is a medical device manufactured by Deep Breathe, Inc.. It received FDA 510(k) clearance on 2025-10-06 under approval number K252007. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BlineSlide?

BlineSlide is a medical device that received FDA 510(k) clearance on 2025-10-06. It is manufactured by Deep Breathe, Inc.. The 510(k) number is K252007.

When was BlineSlide approved by the FDA?

BlineSlide received FDA 510(k) clearance on 2025-10-06, under approval number K252007.

What company makes BlineSlide?

BlineSlide is manufactured by Deep Breathe, Inc..

What is the FDA product code for BlineSlide?

The FDA product code for BlineSlide is QIH.

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Official Source

View on FDA Database →

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