# K031492: Mossmed Dual Intermittent Aspirator

- Pathway: 510(k) (Traditional)
- Applicant: Moss Medical Products
- Decided: Feb 5, 2004 after 269 days
- Product code: KNT (Tubes, Gastrointestinal (And Accessories))
- Device class: 2
- Regulation: 21 CFR 876.5980
- 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 K951423 (1995). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K951423: Aspirator, Continuous & Programmable Intermittent, Impact Instrumentation, Inc. (1995) Summary page 1.

## Indications for use
rhe proposed device interrupts externally supplied continuous suction to individually provide "intermittent suction" to one or two aspiration catheters positioned in the patient's gastrointuestinal tract.

Source page: https://510kreport.com/device/K031492
Methodology: https://510kreport.com/methodology