Cairco , Ltd.: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Cairco , Ltd.” (first 1981, latest 1982), across 6 product codes in 3 review panels. Median 510(k) review time under this name: 78 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 |
|---|---|---|---|
| CBK | Ventilator, Continuous, Facility Use | 3 | 3 |
| BZK | Spirometer, Monitoring (W/Wo Alarm) | 2 | 2 |
| BTT | Humidifier, Respiratory Gas, (Direct Patient Interface) | 1 | 1 |
| CAP | Monitor, Airway Pressure (Includes Gauge And/Or Alarm) | 1 | 1 |
| DWJ | System, Thermal Regulating | 1 | 1 |
| KQX | Goniometer, Ac-Powered | 1 | 1 |
Review panels
- Anesthesiology (7)
- Cardiovascular (1)
- Neurology (1)
Most recent Cairco , Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K812961 | SHEFFIELD INFANT VENTILATOR MARK 4 | CBK | 1982-03-26 | 156 |
| K812957 | EAST AUTOCLAVE HUMIDIFIER | BTT | 1982-03-12 | 142 |
| K812959 | SPIROX A | BZK | 1982-01-22 | 93 |
| K812956 | SPIROX H | BZK | 1982-01-22 | 93 |
| K812958 | EAST-FREEMAN VENTILATOR MARK 2 | CBK | 1982-01-07 | 78 |
| K812955 | EAST WATER UNIT MARK 3 | DWJ | 1981-12-29 | 69 |
| K812953 | RADCLIFFE VENTILATOR MARK 5 | CBK | 1981-11-27 | 37 |
| K812960 | EAST VENTILARM PRESSURE MONITOR ALARM S. | CAP | 1981-11-16 | 26 |
| K810640 | POLARISED LIGHT GRONIOMETER | KQX | 1981-04-17 | 38 |
Recalls
openFDA lists no recalls under a recalling firm named Cairco , Ltd..
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 Cairco , Ltd.?
FDA lists 9 510(k) clearances under the applicant name “Cairco , Ltd.” (first 1981, latest 1982), across 6 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 Cairco , Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Cairco , Ltd. is 78 days.
Which FDA product codes appear under Cairco , Ltd.?
The most frequent FDA product codes under this applicant name are CBK (Ventilator, Continuous, Facility Use, 3); BZK (Spirometer, Monitoring (W/Wo Alarm), 2); BTT (Humidifier, Respiratory Gas, (Direct Patient Interface), 1).
Next steps
- See all 9 Cairco , Ltd. clearances with predicates and recalls
- Run predicate analysis for product code CBK, Cairco , Ltd.'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.