# K050998: Confluent Surgical Micromyst Applicator and Air Pump, Models 20-5000, AP-a-6063

- Pathway: 510(k) (Traditional)
- Applicant: Confluent Surgical,Inc
- Decided: Jun 15, 2005 after 56 days
- Product code: FMF (Syringe, Piston)
- Device class: 2
- Regulation: 21 CFR 880.5860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K964597 (1997). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K994023: Haemacure Hemamyst Surgical Applicator System H-AS01, Haemacure Corp. (2000) Summary page 2.
- K012868: Micromedics Fibrijet Aerosol Applicator, Micromedics, Inc. (2001) Summary page 2.

## Most influential descendants
- K070814: Modification to Confluent Surgical Micromyst Applicator and Air Pump (2007), 0 descendants of its own

## Indications for use
The Confluent Surgical MicroMyst Applicator and Air Pump is indicated for use in the simultaneous delivery of two non-homogenous fluids or solutions onto a surgical site.

Source page: https://510kreport.com/device/K050998
Methodology: https://510kreport.com/methodology