# Physio Technology, Inc.

- Location (FDA's records): Topeka, KS
- FDA decisions: 10 (1984–1988): 10 510(k) clearances
- Product codes: IPF (3), IMG (2), LIH (1), IMI (1), ISA (1), IMJ (1), HCC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- General Project S.R.L.: 1 (https://510kreport.com/company/general-project)
- Lpg USA, Inc.: 1 (https://510kreport.com/company/lpg-usa)

## Its most-cited devices
- K850851: G5 Apparatus T, K1, K3 & the President Model's (1985), cited by 1
- K883893: Omnisound (TM) 3000 (1988), cited by 1

## Recent decisions
- K883893: Omnisound (TM) 3000 (Nov 1, 1988)
- K874076: Modified Omnistim (TM) Electrical Muscle Stimulator (Jan 4, 1988)
- K861039: Omnivac (Vacuum Electrode System) (Sep 26, 1986)
- K850850: Automove/Omnistim IV-Electrical Muscle Stimulator (Jul 1, 1985)
- K850851: G5 Apparatus T, K1, K3 & the President Model's (Jun 25, 1985)
- K850849: Myometer Emg Biofeedback Device (May 31, 1985)
- K843372: Omnisound Therapy Unit (Sep 18, 1984)
- K843351: Omnistim II Combin. Therapy Sys (Sep 18, 1984)

Source page: https://510kreport.com/company/physio-technology