# K012006: Medical Depot Power Neb 1

- Pathway: 510(k) (Special)
- Applicant: Medical Depot, Inc.
- Decided: Jul 13, 2001 after 16 days
- Product code: CAF (Nebulizer (Direct Patient Interface))
- Device class: 2
- Regulation: 21 CFR 868.5630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K862628 (1986). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K003344: Medical Depot Nebulizer, Model Power Neb 2, Medical Depot, Inc. (2001) Summary page 1.
- K862628: Bunn Model 510 Medication Compressor, The John Bunn Co. (1986) Summary page 1.

## Indications for use
The Medical Depot is intended to provide a source of compressed air for medical purposes for use in home health care. This device is used in conjunction with a pneumatic nebulizer to produce a fine aerosol mist of medication for respiratory therapy, for both children and adults suffering from respiratory disorders.

Source page: https://510kreport.com/device/K012006
Methodology: https://510kreport.com/methodology