Cgr Medical Corp.
Mchenry, IL, US
Cgr Medical Corp. appears in FDA device records in Mchenry, IL. FDA records list 20 510(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
- 20
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 20 510(k) clearances for Cgr Medical Corp. between 1978 and 1984. The busiest year on record is 1983, with 6. The most recent is 1984, with 5.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1978 | 1 |
| 1980 | 2 |
| 1981 | 5 |
| 1982 | 1 |
| 1983 | 6 |
| 1984 | 5 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K843926 | PRESTILIX 1690 | IXR | Substantially Equivalent | |
| K843235 | STENOSCOP | JAA | Substantially Equivalent | |
| K843985 | SUSPENSION 7 | Substantially Equivalent | ||
| K841649 | MAXIMAX - 4 | IZP | Substantially Equivalent | |
| K833223 | SONEL 3000A | IYO | Substantially Equivalent | |
| K834306 | PHASIX-HIGH FREQUENCY GENERATOR | ITY | Substantially Equivalent | |
| K833941 | ORION | IYE | Substantially Equivalent | |
| K833846 | PROCESS 100 ST | IZO | Substantially Equivalent | |
| K837465 | ALCYON ROTATIONAL COBALT THERAPY | Substantially Equivalent | ||
| K837412 | SATURNE I LINEAR ACCELERATOR | Substantially Equivalent | ||
| K837336 | VERASUN RADIATION THERAPY SIMULATION SYSTEM | Substantially Equivalent | ||
| K827489 | HYPERLUX 30 IMAGE SYSTEM | JAA | Substantially Equivalent | |
| K813051 | COMPTAR III | IZO | Substantially Equivalent | |
| K812963 | IBIS II | JAA | Substantially Equivalent | |
| K812238 | D.I.V.A.S. | IZI | Substantially Equivalent | |
| K811723 | WHOLE BODY SCANNER | JAK | Substantially Equivalent | |
| K810945 | SCANEL 100 | IYO | Substantially Equivalent | |
| K802704 | SIAM 80-INSTANTANEOUS SONOGRAPH W/STOR. | IYO | Substantially Equivalent | |
| K801844 | SONIA-SO NOGRAPH-NUMERICAL ANALYSIS | IYO | Substantially Equivalent | |
| K781040 | CT SCANNER ND 8000 | JAK | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- IYEAccelerator, Linear, Medical
- ITYAssembly, Tube Housing, X-Ray, Diagnostic
- IZOGenerator, High-Voltage, X-Ray, Diagnostic
- IZPProgrammer, Changer, Film/Cassette, Radiographic
- IYOSystem, Imaging, Pulsed Echo, Ultrasonic
- IZISystem, X-Ray, Angiographic
- JAASystem, X-Ray, Fluoroscopic, Image-Intensified
- JAKSystem, X-Ray, Tomography, Computed
- IXRTable, Radiographic, Tilting
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.
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Data as of , FDA export datePage updated Source: openFDA, public domain