Research Industries Corp.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Research Industries Corp.” (first 1983, latest 1995), across 4 product codes in 2 review panels. Median 510(k) review time under this name: 85 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 |
|---|---|---|---|
| DWF | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass | 2 | 2 |
| DQY | Catheter, Percutaneous | 1 | 1 |
| DTL | Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass | 1 | 1 |
| FPA | Set, Administration, Intravascular | 1 | 1 |
Review panels
- Cardiovascular (4)
- General Hospital (1)
Most recent Research Industries Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K945931 | RMI CIRKUIT-GUARD(TM) PRESSURE RELIEF VALVE | DTL | 1995-03-03 | 88 |
| K833433 | PHYSIO-PROBE-HIGH PERMEABILITY CATH. | DQY | 1983-12-29 | 85 |
| K832542 | I.V. ADMINISTRATION SET | FPA | 1983-10-31 | 94 |
| K831769 | VARIOUS CARDIOVASCULAR SURGICAL DEVICE | DWF | 1983-08-12 | 72 |
| K831759 | INTRACARDIA SUCKERS | DWF | 1983-08-12 | 72 |
Recalls
openFDA lists no recalls under a recalling firm named Research Industries Corp..
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.
- Research Medical, Inc. (35 510(k)s)
- Research Instruments , Ltd. (9 510(k)s)
- Research Development Corp. (6 510(k)s)
- Research Diagnostics, Inc. (3 510(k)s)
- Research Consultants, Inc. (1 510(k)s)
- Research Endoscope Systems Intl. (1 510(k)s)
- Research Instrumentation Associates, Inc. (1 510(k)s)
- Research Surgical Systems (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Research Industries Corp.?
FDA lists 5 510(k) clearances under the applicant name “Research Industries Corp.” (first 1983, latest 1995), across 4 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 Research Industries Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Research Industries Corp. is 85 days.
Which FDA product codes appear under Research Industries Corp.?
The most frequent FDA product codes under this applicant name are DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass, 2); DQY (Catheter, Percutaneous, 1); DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass, 1).
Next steps
- See all 5 Research Industries Corp. clearances with predicates and recalls
- Run predicate analysis for product code DWF, Research Industries Corp.'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 (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.