Will Ross Co.: FDA clearances and approvals
Will Ross Co. has 14 FDA 510(k) clearances (first 1976, latest 1978), across 13 product codes in 4 review panels. Median 510(k) review time: 8 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 |
|---|---|---|---|
| INT | Plinth | 2 | 2 |
| BSY | Catheters, Suction, Tracheobronchial | 1 | 1 |
| BTO | Tube, Tracheostomy (W/Wo Connector) | 1 | 1 |
| CCE | Analyzer, Gas, Oxygen, Partial Pressure, Blood-Phase, Indwelling | 1 | 1 |
| EXR | Urinometer, Mechanical | 1 | 1 |
| FRC | Indicator, Biological Sterilization Process | 1 | 1 |
| FRL | Fiber, Medical, Absorbent | 1 | 1 |
| ILZ | Accessories, Traction | 1 | 1 |
| IOE | Bars, Parallel, Exercise | 1 | 1 |
| IQI | Orthosis, Limb Brace | 1 | 1 |
Plus 3 more product codes.
Review panels
Most recent Will Ross Co. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K780850 | SEARLE NEONATAL OXYGEN PROBE | CCE | 1978-08-23 | 93 |
| K771561 | DOVER URINE METER | EXR | 1977-09-07 | 23 |
| K771132 | KENWOOD BIOLOGICAL STEOILIZ. INDICATOR | FRC | 1977-07-14 | 21 |
| K770612 | SPLINT, BOHLER | IQI | 1977-04-08 | 8 |
| K770611 | PARALLEL BARS | IOE | 1977-04-08 | 8 |
| K770610 | TABLE, TREATMENT & TRACTION, HI-LO | ITH | 1977-04-08 | 8 |
| K770609 | TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT | INT | 1977-04-08 | 8 |
| K770608 | WALKING AID | ITJ | 1977-04-08 | 8 |
| K770607 | TRACTION HARNESS | ILZ | 1977-04-08 | 8 |
| K770509 | TABLE, MASSAGE AND TREATMENT | INT | 1977-04-05 | 19 |
4 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Will Ross 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 Will Ross Co. have?
Will Ross Co. has 14 FDA 510(k) clearances (first 1976, latest 1978), across 13 product codes in 4 review panels.
How long does FDA take to clear Will Ross Co.'s 510(k)s?
The median time from FDA receipt to decision across Will Ross Co.'s cleared 510(k)s is 8 days.
What devices does Will Ross Co. make?
Its most frequent FDA product codes are INT (Plinth, 2); BSY (Catheters, Suction, Tracheobronchial, 1); BTO (Tube, Tracheostomy (W/Wo Connector), 1).
Has Will Ross Co. had device recalls?
openFDA lists no recalls under a recalling firm name matching Will Ross Co. Related entities may recall under other names.
Next steps
- See all 14 Will Ross Co. clearances with predicates and recalls
- Run predicate analysis for product code INT, Will Ross 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.