Ria Products, Inc.: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Ria Products, Inc.” (first 1978, latest 1981), across 6 product codes in 1 review panel. Median 510(k) review time under this name: 44 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 |
|---|---|---|---|
| CDD | Radioassay, Vitamin B12 | 3 | 3 |
| CGN | Acid, Folic, Radioimmunoassay | 2 | 2 |
| CGR | Radioimmunoassay, Cortisol | 1 | 1 |
| JJA | Radio-Labeled Iron Method, Iron (Non-Heme) | 1 | 1 |
| JMG | Radioimmunoassay (Two-Site Solid Phase), Ferritin | 1 | 1 |
| JQG | Radiometric, Fe59, Iron Binding Capacity | 1 | 1 |
Review panels
Most recent Ria Products, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K813310 | NO-HOIL COMBOSTAT II KIT | CDD | 1981-12-17 | 23 |
| K802969 | CORTISOL 125-I RADIOIMMUNOASSAY KIT | CGR | 1981-01-02 | 42 |
| K801579 | VITAMIN B12 - NO-BOIL KIT | CDD | 1980-10-23 | 106 |
| K801578 | COMBOSTAT - NO-BOIL KIT | CDD | 1980-10-23 | 106 |
| K800710 | FERRITIRON KIT CAT. #RP-1100 | JQG | 1980-05-14 | 44 |
| K800914 | NO-BOIL FOLATE KIT #RP-500 | CGN | 1980-05-08 | 17 |
| K781844 | FERRITIN KIT | JMG | 1979-01-10 | 70 |
| K781769 | IRON 59 KIT | JJA | 1978-12-04 | 49 |
| K780148 | RIA FOR FOLATES & VIT. B12, COMBO KIT | CGN | 1978-03-03 | 32 |
Recalls
openFDA lists no recalls under a recalling firm named Ria Products, 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 Ria Products, Inc.?
FDA lists 9 510(k) clearances under the applicant name “Ria Products, Inc.” (first 1978, latest 1981), across 6 product codes 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 Ria Products, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Ria Products, Inc. is 44 days.
Which FDA product codes appear under Ria Products, Inc.?
The most frequent FDA product codes under this applicant name are CDD (Radioassay, Vitamin B12, 3); CGN (Acid, Folic, Radioimmunoassay, 2); CGR (Radioimmunoassay, Cortisol, 1).
Next steps
- See all 9 Ria Products, Inc. clearances with predicates and recalls
- Run predicate analysis for product code CDD, Ria Products, 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.