# K112890: Normatec MVP

- Pathway: 510(k) (Traditional)
- Applicant: NormaTec Industries, LP
- Decided: Jan 4, 2012 after 96 days
- Product code: IRP (Massager, Powered Inflatable Tube)
- Device class: 2
- Regulation: 21 CFR 890.5650
- 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 K810338 (1981). 8 ancestors in all.
52 later devices descend from it; 1 cites it directly.
0 of 61 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K013436: Normatec PCD, Normatec, Inc. (2001)
- K032505: Air Press Massager, Telebrands Corp (2003) Summary page 1.
- K000655: Ppcid- Pneumatic Peripheral Circulation Improvement (Footrest) Device, Ahava Stein (2001) Summary page 2.

## Most influential descendants
- K160608: NormaTec Pulse and NormaTec Pulse Pro (2016), 51 descendants of its own
- K182668: Rapid Reboot Compression Therapy System (2018), 38 descendants of its own
- K193354: Air Compression Therapy Device (2020), 20 descendants of its own
- K183169: Pulse 2.0, Pulse Pro 2.0 (2018), 10 descendants of its own
- K220217: Normatec 3 (2022), 7 descendants of its own

## Indications for use
The NormaTec MVP is an air pressure massager intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas.

Source page: https://510kreport.com/device/K112890
Methodology: https://510kreport.com/methodology