Radiation Technology, Inc.: FDA filings under this applicant name
FDA lists 7 510(k) clearances under the applicant name “Radiation Technology, Inc.” (first 1980, latest 1991), across 5 product codes in 3 review panels. Median 510(k) review time under this name: 24 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 |
|---|---|---|---|
| JSG | Culture Media, Non-Selective And Non-Differential | 2 | 2 |
| JSH | Culture Media, Non-Selective And Differential | 2 | 2 |
| JAI | Couch, Radiation Therapy, Powered | 1 | 1 |
| JJH | Clinical Sample Concentrator | 1 | 1 |
| JTZ | Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth | 1 | 1 |
Review panels
- Microbiology (5)
- Clinical Chemistry (1)
- Radiology (1)
Most recent Radiation Technology, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K910648 | THERAPY CHAIR SYSTEM | JAI | 1991-07-22 | 158 |
| K802892 | CULTURE MEDIA FOR IN VITRO DIAG. USE | JSG | 1980-12-11 | 24 |
| K801943 | BRAIN HEART INFUSION MICROBIOLOGICAL | JSG | 1980-09-09 | 26 |
| K801817 | MICROBIOLOGY CULTURE MEDIA, C.L.E.D. | JSH | 1980-08-27 | 27 |
| K801901 | MUELLER HINTON AGAR | JTZ | 1980-08-20 | 12 |
| K801772 | MICROBIOLOGY CULTURE MEDIA-MACCONKEY AG | JJH | 1980-08-20 | 23 |
| K801847 | TRIPLE SUGAR IRON AGAR(MICRO/CULT/MEDIA | JSH | 1980-08-13 | 9 |
Recalls
openFDA lists no recalls under a recalling firm named Radiation Technology, 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.
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.
- Radiation Measurements, Inc. (12 510(k)s)
- Radiation Products Design, Inc. (8 510(k)s)
- Radiation Development Co., Inc. (2 510(k)s)
- Radiation Monitoring Devices, Inc. (2 510(k)s)
- Radiation Oncology Computer Systems (2 510(k)s)
- Radiation Safety & Nuclear Products, Inc. (2 510(k)s)
- Radiation Products, LLC (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Radiation Technology, Inc.?
FDA lists 7 510(k) clearances under the applicant name “Radiation Technology, Inc.” (first 1980, latest 1991), across 5 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 Radiation Technology, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Radiation Technology, Inc. is 24 days.
Which FDA product codes appear under Radiation Technology, Inc.?
The most frequent FDA product codes under this applicant name are JSG (Culture Media, Non-Selective And Non-Differential, 2); JSH (Culture Media, Non-Selective And Differential, 2); JAI (Couch, Radiation Therapy, Powered, 1).
Next steps
- See all 7 Radiation Technology, Inc. clearances with predicates and recalls
- Run predicate analysis for product code JSG, Radiation Technology, 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.