# K013306: Minime Nasal Mask, Model P/N 50220

- Pathway: 510(k) (Special)
- Applicant: Sleepnet Corporation
- Decided: Nov 2, 2001 after 29 days
- Product code: BZD (Ventilator, Non-Continuous (Respirator))
- Device class: 2
- Regulation: 21 CFR 868.5905
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K090935: Minime Pediatric Mask (2009), 5 descendants of its own
- K102224: Pixi Pediatric Mask (2010), 3 descendants of its own
- K120920: Hsiner Cpap Silicone Nasal Mask Size XS/Petite  Hsiner Nasal Pillow Mask Hsiner Infant Cpap Cannula (2012), 1 descendant of its own
- K243225: Nasal Pillow Mask - Small (NNPM-01/ Nefes S); Nasal Pillow Mask - Medium (NNPM-02/ Nefes M); Nasal Pillow Mask - Large (NNPM-03/ Nefes L) (2024), 0 descendants of its own
- K151683: SleepWeaver Advance Pediatric Nasal CPAP Mask (2016), 0 descendants of its own

## Indications for use
The SleepNet Corporation MiniMe™ Nasal Mask is intended to be used with positive airway pressure devices such as CPAP (Continuous Positive Airway Pressure), operating at or above 3 cmHO for the treatment of adult obstructive sleep apnea.

Source page: https://510kreport.com/device/K013306
Methodology: https://510kreport.com/methodology