General Physiotherapy, Inc.: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “General Physiotherapy, Inc.” (first 1981, latest 1987), across 5 product codes in 2 review panels. Median 510(k) review time under this name: 29 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| ISA | Massager, Therapeutic, Electric | 5 | 5 |
| BYI | Percussor, Powered-Electric | 1 | 1 |
| CCQ | Nebulizer, Medicinal, Non-Ventilatory (Atomizer) | 1 | 1 |
| IPF | Stimulator, Muscle, Powered | 1 | 1 |
| IRO | Vibrator, Therapeutic | 1 | 1 |
Review panels
- Physical Medicine (7)
- Anesthesiology (2)
Most recent General Physiotherapy, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K870939 | VIBRACARE | ISA | 1987-04-06 | 28 |
| K863383 | FACIAL MASSAGER, BATTERY POWERED | ISA | 1986-09-15 | 12 |
| K861834 | THERACUSHION MODEL 1000 | ISA | 1986-05-27 | 14 |
| K855129 | NEOCUSSOR (MASSAGER, BATTERY) POWERED | BYI | 1986-01-23 | 31 |
| K853710 | THERACUSHION | ISA | 1986-01-03 | 120 |
| K852944 | FLEXIMATIC MASSAGER | ISA | 1985-09-05 | 56 |
| K850047 | SANYO ELECTRONIC MUSCLE STIMULATORS | IPF | 1985-03-05 | 56 |
| K844591 | MIST-EASE NEBULIZER | CCQ | 1984-12-13 | 17 |
| K810244 | PORTA-PULS MUSCLE STIMULATOR | IRO | 1981-02-26 | 29 |
Recalls
openFDA lists no recalls under a recalling firm named General Physiotherapy, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- General Electric Co. (254 510(k)s)
- General Diagnostics (39 510(k)s)
- General Electric Medical Systems Information Techn (33 510(k)s)
- General Biometrics, Inc. (23 510(k)s)
- General Medical Co. (15 510(k)s)
- General Surgical Innovations (14 510(k)s)
- General X-Ray, Inc. (14 510(k)s)
- General Devices (13 510(k)s)
- General Medical Merate S.P.A (7 510(k)s)
- General Theraphysical, Inc. (7 510(k)s)
- General Atomics (6 510(k)s)
- General Electric Medical Systems (6 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under General Physiotherapy, Inc.?
FDA lists 9 510(k) clearances under the applicant name “General Physiotherapy, Inc.” (first 1981, latest 1987), across 5 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by General Physiotherapy, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name General Physiotherapy, Inc. is 29 days.
Which FDA product codes appear under General Physiotherapy, Inc.?
The most frequent FDA product codes under this applicant name are ISA (Massager, Therapeutic, Electric, 5); BYI (Percussor, Powered-Electric, 1); CCQ (Nebulizer, Medicinal, Non-Ventilatory (Atomizer), 1).
Next steps
- See all 9 General Physiotherapy, Inc. clearances with predicates and recalls
- Run predicate analysis for product code ISA, General Physiotherapy, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.