# K954171: Arco-MBC, Arco MC

- Pathway: 510(k) (Traditional)
- Applicant: Holl Meditronics, Inc.
- Decided: Apr 30, 1996 after 238 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
29 later devices descend from it; 1 cites it directly.
0 of 30 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
- K993265: Soring GMBH, Arco 3000, Arco 2000, Arco 1000, MBC 601, MBC 600 (1999), 28 descendants of its own
- K024059: MBC Series (2003), 26 descendants of its own
- K052859: Aquamantys Pump Generator System (2005), 24 descendants of its own
- K063639: Aquamantys SS4.0 Bipolar Sealer, Model 23-121-1 (2007), 7 descendants of its own
- K111732: Aquamantys SBS 5.0 Sheated Biopolar Sealer (2011), 5 descendants of its own

Source page: https://510kreport.com/device/K954171
Methodology: https://510kreport.com/methodology