Research Development Corp.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Research Development Corp.” (first 1977, latest 1987), across 4 product codes in 3 review panels. Median 510(k) review time under this name: 13 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 |
|---|---|---|---|
| BZQ | Monitor, Breathing Frequency | 2 | 2 |
| JAX | Pneumotachometer | 2 | 2 |
| KLA | Monitor, Esophageal Motility, Anorectal Motility, And Tube | 1 | 1 |
| KWP | Appliance, Fixation, Spinal Interlaminal | 1 | 1 |
Review panels
Most recent Research Development Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K871870 | HSC UNIT ROD | KWP | 1987-07-21 | 69 |
| K791730 | RING-ORIFICE, TURBULENT FLOW PNEUMOT | JAX | 1979-11-16 | 80 |
| K771407 | LUNG VOLUME & PRESSURE MONITOR | BZQ | 1977-08-04 | 6 |
| K771019 | LUNG-MECHANICS MONITOR | BZQ | 1977-06-14 | 8 |
| K770785 | MONITOR, RESPIRATORY, TWO-GAS, RDC | KLA | 1977-05-20 | 18 |
| K770061 | VO RESPIRATORY PNEUMOTACHOGRAPH | JAX | 1977-01-14 | 3 |
Recalls
openFDA lists no recalls under a recalling firm named Research Development 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 Industries Corp. (5 510(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 Development Corp.?
FDA lists 6 510(k) clearances under the applicant name “Research Development Corp.” (first 1977, latest 1987), across 4 product codes in 3 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 Development Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Research Development Corp. is 13 days.
Which FDA product codes appear under Research Development Corp.?
The most frequent FDA product codes under this applicant name are BZQ (Monitor, Breathing Frequency, 2); JAX (Pneumotachometer, 2); KLA (Monitor, Esophageal Motility, Anorectal Motility, And Tube, 1).
Next steps
- See all 6 Research Development Corp. clearances with predicates and recalls
- Run predicate analysis for product code BZQ, Research Development 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.