# K933902: Moblvac Iii

- Pathway: 510(k) (Traditional)
- Applicant: Aeros Instruments, Inc.
- Decided: May 20, 1994 after 283 days
- Product code: BTA (Pump, Portable, Aspiration (Manual Or Powered))
- Device class: 2
- Regulation: 21 CFR 878.4780
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
94 later devices descend from it; 1 cites it directly.
0 of 95 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K043544: Medela Dominant 35 C/I Secretion and Surgical Aspirator (2005), 93 descendants of its own
- K061205: Medela Vario 8/18/CI Secretion & Surgical Aspirator (2006), 85 descendants of its own
- K080357: Medela Invia Wound Therapy (2008), 75 descendants of its own
- K083375: Renasys GO Negative Pressure Wound Therapy (2009), 56 descendants of its own
- K111170: PICO (2011), 26 descendants of its own

## Recalls of this device
- Nov 16, 2021 · Class II · Z-0482-2022: Increase in premature device failures

Source page: https://510kreport.com/device/K933902
Methodology: https://510kreport.com/methodology