Cryosan, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Cryosan, Inc.” (first 1981, latest 1983), across 5 product codes in 2 review panels. Median 510(k) review time under this name: 36 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 |
|---|---|---|---|
| KZL | Device, Warming. Blood And Plasma | 2 | 2 |
| FIR | Pump, Blood, Extra-Luminal | 1 | 1 |
| GIF | Diluent, Blood Cell | 1 | 1 |
| GKT | Separator, Automated, Blood Cell, Diagnostic | 1 | 1 |
| LKN | Separator, Automated, Blood Cell And Plasma, Therapeutic | 1 | 1 |
Review panels
Most recent Cryosan, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K831953 | INFUSION PUMP | FIR | 1983-07-19 | 34 |
| K830831 | AUTOMATED BLOOD CELL SEPARATOR | LKN | 1983-06-16 | 92 |
| K822521 | AUTOMATED BLOOD CELL SEPARATOR | GKT | 1982-09-30 | 38 |
| K813489 | ROCKING/CIRCULATING CYTO-THERM II 3570 | KZL | 1982-03-04 | 93 |
| K812311 | CIRCULATING CYTO-THERMS | KZL | 1981-09-16 | 30 |
| K812309 | CRYOSAN NORMAL SALINE | GIF | 1981-09-16 | 30 |
Recalls
openFDA lists no recalls under a recalling firm named Cryosan, 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 Cryosan, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Cryosan, Inc.” (first 1981, latest 1983), across 5 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 Cryosan, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Cryosan, Inc. is 36 days.
Which FDA product codes appear under Cryosan, Inc.?
The most frequent FDA product codes under this applicant name are KZL (Device, Warming. Blood And Plasma, 2); FIR (Pump, Blood, Extra-Luminal, 1); GIF (Diluent, Blood Cell, 1).
Next steps
- See all 6 Cryosan, Inc. clearances with predicates and recalls
- Run predicate analysis for product code KZL, Cryosan, 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 (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.