Quickie Designs, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Quickie Designs, Inc.” (first 1990, latest 1997), across 1 product code in 1 review panel. Median 510(k) review time under this name: 244 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 |
|---|---|---|---|
| ITI | Wheelchair, Powered | 6 | 6 |
Review panels
Most recent Quickie Designs, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K972230 | QUICKIE P90 SERIES | ITI | 1997-12-02 | 172 |
| K963385 | QUICKIE POWER WHEELCHAIRS P200 SERIES | ITI | 1997-04-28 | 244 |
| K963382 | QUICKIE P100 SERIES | ITI | 1997-04-28 | 244 |
| K963381 | QUICKIE P300 SERIES | ITI | 1997-04-28 | 244 |
| K924278 | QUICKIE P200 | ITI | 1994-03-28 | 580 |
| K900330 | QUICKIE P300 WHEELCHAIR | ITI | 1990-02-15 | 23 |
Recalls
openFDA lists no recalls under a recalling firm named Quickie Designs, 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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Quickie Designs, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Quickie Designs, Inc.” (first 1990, latest 1997), across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Quickie Designs, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Quickie Designs, Inc. is 244 days.
Which FDA product codes appear under Quickie Designs, Inc.?
The most frequent FDA product codes under this applicant name are ITI (Wheelchair, Powered, 6).
Next steps
- See all 6 Quickie Designs, Inc. clearances with predicates and recalls
- Run predicate analysis for product code ITI, Quickie Designs, 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.