# K895761: General Asperator

- Pathway: 510(k) (Traditional)
- Applicant: Kolster Methods
- Decided: Oct 18, 1989 after 22 days
- Product code: JCX (Apparatus, Suction, Ward Use, Portable, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 878.4780
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
28 later devices descend from it; 2 cite it directly.
0 of 29 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K980392: Psi-Tec Aspirator (1998), 27 descendants of its own
- K981215: Psi-Tec Liposuction Aspirator (1998), 26 descendants of its own
- K032802: HK Liposuction Aspirator, Model AP-Iii & AP230-Iii (2003), 22 descendants of its own
- K053451: Liposat (Infiltration Pump), Model 00 002 274; Vacusat (Suction Unit), Model 00 002 252 (220 V), 00 002 318 (110 V); (2006), 13 descendants of its own
- K081593: Power Aspirator, Model LS2 or LS2DP (2008), 4 descendants of its own

Source page: https://510kreport.com/device/K895761
Methodology: https://510kreport.com/methodology