RecallHawk

Summary

Deep Breathe, Inc. received 510(k) clearance for BlineSlide, a QIH device. Cleared on 2025-10-06.

Details

Source

510(k) Clearance

External ID

K252007

Action Date

2025-10-06

Status

Traditional

Category

device

Product Code

QIH

Product Description

BlineSlide. Product code: QIH.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Deep Breathe, Inc. have FDA actions?

This is the only FDA action we have on record for Deep Breathe, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K252007" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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