Rhytec Incorporated: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Rhytec Incorporated” (first 2006, latest 2008), across 1 product code in 1 review panel. 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 |
|---|---|---|---|
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 5 | 5 |
Review panels
Most recent Rhytec Incorporated 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K082197 | RHYTEC, INC., PORTRAIT PSR | GEI | 2008-08-22 | 18 |
| K073111 | PORTRAIT PSR, MODEL 745915 | GEI | 2008-03-27 | 143 |
| K072394 | PORTRAIT STAND-OFF | GEI | 2007-09-12 | 16 |
| K071786 | PORTRAIT PSR | GEI | 2007-07-26 | 24 |
| K060948 | PORTRAIT PSR3 | GEI | 2006-09-05 | 152 |
Recalls
openFDA lists no recalls under a recalling firm named Rhytec Incorporated.
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 Rhytec Incorporated?
FDA lists 5 510(k) clearances under the applicant name “Rhytec Incorporated” (first 2006, latest 2008), across 1 product code 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 Rhytec Incorporated?
The median time from FDA receipt to decision across 510(k)s cleared under the name Rhytec Incorporated is 24 days.
Which FDA product codes appear under Rhytec Incorporated?
The most frequent FDA product codes under this applicant name are GEI (Electrosurgical, Cutting & Coagulation & Accessories, 5).
Next steps
- See all 5 Rhytec Incorporated clearances with predicates and recalls
- Run predicate analysis for product code GEI, Rhytec Incorporated'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.