Jason Marketing Co.: FDA clearances and approvals
Jason Marketing Co. has 5 FDA 510(k) clearances (first 1987, latest 1992), across 1 product code in 1 review panel. Median 510(k) review time: 59 days.
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 |
|---|---|---|---|
| DRX | Electrode, Electrocardiograph | 5 | 5 |
Review panels
- Cardiovascular (5)
Most recent Jason Marketing Co. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K924133 | ELECTROTRACE, MODIFICATION | DRX | 1992-10-30 | 87 |
| K903555 | ELECTROTRACE DISPOSABLE AG/AGCL EKG MON. ELEC. | DRX | 1990-11-05 | 90 |
| K896569 | ELECTROTRACE DISPOSABLE AG/AGCL EKG MONITOR ELEC. | DRX | 1990-01-18 | 59 |
| K894679 | ELECTROTRACE DISP. RESTING EKG ELECTRODES | DRX | 1989-09-13 | 50 |
| K871626 | ELECTROTRACE DISP REST EKG ELECTRODE, CAT. ET1200 | DRX | 1987-06-05 | 39 |
Recalls
openFDA lists no recalls under a recalling firm named Jason Marketing Co..
Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.
Frequently asked questions
How many FDA 510(k) clearances does Jason Marketing Co. have?
Jason Marketing Co. has 5 FDA 510(k) clearances (first 1987, latest 1992), across 1 product code in 1 review panel.
How long does FDA take to clear Jason Marketing Co.'s 510(k)s?
The median time from FDA receipt to decision across Jason Marketing Co.'s cleared 510(k)s is 59 days.
What devices does Jason Marketing Co. make?
Its most frequent FDA product codes are DRX (Electrode, Electrocardiograph, 5).
Has Jason Marketing Co. had device recalls?
openFDA lists no recalls under a recalling firm name matching Jason Marketing Co. Related entities may recall under other names.
Next steps
- See all 5 Jason Marketing Co. clearances with predicates and recalls
- Run predicate analysis for product code DRX, Jason Marketing Co.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.