Progressive Electrical Therapeutics: FDA filings under this applicant name
FDA lists 10 510(k) clearances under the applicant name “Progressive Electrical Therapeutics” (first 1991, latest 1995), across 6 product codes in 2 review panels. Median 510(k) review time under this name: 116 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 |
|---|---|---|---|
| IPF | Stimulator, Muscle, Powered | 4 | 4 |
| INW | Table, Mechanical | 2 | 2 |
| BXB | Exerciser, Powered | 1 | 1 |
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief | 1 | 1 |
| INQ | Table, Powered | 1 | 1 |
| JFB | Table, Physical Therapy, Multi Function | 1 | 1 |
Review panels
- Physical Medicine (9)
- Neurology (1)
Most recent Progressive Electrical Therapeutics 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K933197 | THE SIGNATURE SERIES, M IV | GZJ | 1995-06-02 | 701 |
| K943972 | EURO TECH DIAMOND CHIROPRACTIC TABLE | INQ | 1994-10-11 | 57 |
| K943975 | EURO TECH PLATINUM CHIROPRACTIC TABLE | INW | 1994-09-29 | 45 |
| K943974 | EURO TECH MARQUISE CHIROPRACTIC TABLE | INW | 1994-09-29 | 45 |
| K943973 | EURO TECH STERLING ROLLER TABLE | JFB | 1994-09-29 | 45 |
| K933194 | THE SIGNATURE SERIES, IMC IV | IPF | 1994-07-13 | 377 |
| K933196 | THE SIGNATURE SERIES, IC II | IPF | 1994-07-12 | 376 |
| K934919 | THE SIGNATURE SERIES, MAGNUM 100 | IPF | 1994-04-06 | 174 |
| K933195 | THE SIGNATURE SERIES, IC IV | IPF | 1994-02-23 | 237 |
| K914394 | BACK MASTER | BXB | 1991-11-13 | 43 |
Recalls
openFDA lists no recalls under a recalling firm named Progressive Electrical Therapeutics.
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.
- Progressive Dynamics, Inc. (7 510(k)s)
- Progressive Medical Technology, Inc. (5 510(k)s)
- Progressive Concepts, Inc. (4 510(k)s)
- Progressive Productions , Ltd. (4 510(k)s)
- Progressive Surgical Products, Inc. (3 510(k)s)
- Progressive Technology, Inc. (3 510(k)s)
- Progressive Affiliated Labs, Inc. (1 510(k)s)
- Progressive Aligners, Inc. (1 510(k)s)
- Progressive Dental Supply (1 510(k)s)
- Progressive Iv'S, Inc. (1 510(k)s)
- Progressive Medical, Inc. (1 510(k)s)
- Progressive Medical Applications Corp. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Progressive Electrical Therapeutics?
FDA lists 10 510(k) clearances under the applicant name “Progressive Electrical Therapeutics” (first 1991, latest 1995), across 6 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 Progressive Electrical Therapeutics?
The median time from FDA receipt to decision across 510(k)s cleared under the name Progressive Electrical Therapeutics is 116 days.
Which FDA product codes appear under Progressive Electrical Therapeutics?
The most frequent FDA product codes under this applicant name are IPF (Stimulator, Muscle, Powered, 4); INW (Table, Mechanical, 2); BXB (Exerciser, Powered, 1).
Next steps
- See all 10 Progressive Electrical Therapeutics clearances with predicates and recalls
- Run predicate analysis for product code IPF, Progressive Electrical Therapeutics'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.