# K092999: NBP Cuff

- Pathway: 510(k) (Traditional)
- Applicant: Draeger Medical AG & Co. KG
- Decided: Nov 24, 2009 after 57 days
- Product code: DXQ (Blood Pressure Cuff)
- Device class: 2
- Regulation: 21 CFR 870.1120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K946306 (1995). 25 ancestors in all.
No later device cites it as a predicate yet.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022889: Siemens Infinity Modular Monitors, Models SC 8000, SC 7000 & SC 9000XL & Siemens Infinity Explorer, Siemens Medical Solutions USA, Inc. (2002) Summary page 2.
- K022482: Sensa-Cuff, Models Infant, Child, Adult, Ge Medical Systems Information Technologies (2002) Summary page 2.
- K974080: Critikon Soft Blood Pressure Cuff, Johnson & Johnson Medical, Inc. (1998) Summary page 2.
- K991525: Deroyal Sterile Neonatal Blood Pressure Cuff, Deroyal Industries, Inc. (1999) Summary page 2.
- (no number) Critikon Dura-Cuf: named in the summary without a submission number

## Indications for use
Drfger cuffs are intended to be used for automatic non-invasive blood pressure measurement. Drfger cuffs are compatible with Dr/ger and Siemens patient monitors. Neonatal cuffs are designed for single-patient use.

Source page: https://510kreport.com/device/K092999
Methodology: https://510kreport.com/methodology