# K101719: Tacamo Manual Wheelchair

- Pathway: 510(k) (Abbreviated)
- Applicant: Dalton Instrument Corp.
- Decided: Aug 25, 2010 after 68 days
- Product code: IOR (Wheelchair, Mechanical)
- Device class: 1
- Regulation: 21 CFR 890.3850
- 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 K941989 (1994). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K984447: Model Action at II Manual Wheelchair, Invacare Corp. (1999) Summary page 1.
- K952641: Quickie TSR, Sunrise Medical, Inc. (1995) Summary page 1.

## Indications for use
The intended use of the TACAMO Manual Wheelchair is to provide mobility to persons limited to a sitting position.

Source page: https://510kreport.com/device/K101719
Methodology: https://510kreport.com/methodology