Castle Co.
Mchenry, IL, US
Castle Co. appears in FDA device records in Mchenry, IL. FDA records list 21 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 21
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 21 510(k) clearances for Castle Co. between 1976 and 1987. The busiest year on record is 1977, with 8. The most recent is 1987, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1976 | 1 |
| 1977 | 8 |
| 1978 | 3 |
| 1979 | 1 |
| 1980 | 2 |
| 1983 | 2 |
| 1984 | 1 |
| 1985 | 1 |
| 1986 | 1 |
| 1987 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K870975 | MODIFIED CASTLE POWERCLAVE | FLE | Substantially Equivalent | |
| K860263 | CASTLE 7538 FLOOR LOADING WASHER | LDS | Substantially Equivalent | |
| K844089 | CASTLE 7515 UTENSIL/GLASSWARE WASHER | LDS | Substantially Equivalent | |
| K834048 | BOVIE CONDUCTIVE ADHES-DISPER-ELECTRO | GEI | Substantially Equivalent | |
| K833074 | CASTLE TEC-TEST S.M.A.R.T. PACK | JOJ | Substantially Equivalent | |
| K831595 | CASTLE MODEL 3341 & 3441 & 4141 GAS AER | FLI | Substantially Equivalent | |
| K792660 | 1500 EO EXHAUST HOOD | FLF | Substantially Equivalent | |
| K792649 | UNISPORE-BIOLOGICAL INDICATORS | FRC | Substantially Equivalent | |
| K790677 | EO EVACUATING SYSTEM I | FLI | Substantially Equivalent | |
| K781887 | 9100 DAYSTAR AND 9110 ORBITER PACKAGE | FSY | Substantially Equivalent | |
| K781484 | CASTLE MODEL 3146 GAS AERATOR | FLI | Substantially Equivalent | |
| K780666 | DAYSTAR SELECTRA & SELECTRA/ORBITER | FSY | Substantially Equivalent | |
| K771865 | DAYSTAR SURG. LIGHT 9100 & ORBITER 9110 | FSY | Substantially Equivalent | |
| K771229 | STERILIZERS, 3100 SERIES TRIM LINE | FLE | Substantially Equivalent | |
| K770953 | MONITOR, AERATION, TEC-TEST | FRC | Substantially Equivalent | |
| K770682 | STERILIZER, SERIES 3000, MODIFICATION TO | FLE | Substantially Equivalent | |
| K770536 | STEAM STERILIZER, 3000 | FLE | Substantially Equivalent | |
| K770372 | STERILIZER, STEAM, CASTLE 3000 | FLE | Substantially Equivalent | |
| K770078 | CASTLE TEC-TEST STEAM STERI. INTEGRATOR | JOJ | Substantially Equivalent | |
| K761015 | MARKET CASTLE UNISPHERE | FRC | Substantially Equivalent | |
| K761011 | CASTLE TEC-TEST AERATION MONITOR | JOJ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- FLICabinet, Ethylene-Oxide Gas Aerator
- LDSDevice, Pasteurization, Hot Water
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- FRCIndicator, Biological Sterilization Process
- JOJIndicator, Physical/Chemical Sterilization Process
- FSYLight, Surgical, Ceiling Mounted
- FLFSterilizer, Ethylene-Oxide Gas
- FLESterilizer, Steam
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
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Data as of , FDA export datePage updated Source: openFDA, public domain
