The following data is part of a premarket notification filed by Cgr Medical Corp. with the FDA for D.i.v.a.s..
| Device ID | K812238 |
| 510k Number | K812238 |
| Device Name: | D.I.V.A.S. |
| Classification | System, X-ray, Angiographic |
| Applicant | CGR MEDICAL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IZI |
| CFR Regulation Number | 892.1600 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-08-11 |
| Decision Date | 1981-09-11 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() D.I.V.A.S. 85659877 4308195 Dead/Cancelled |
Divorcing Independent Very Able Survivors, LLC 2012-06-24 |
![]() D.I.V.A.S. 73336575 1221544 Dead/Cancelled |
CGR Medical Corporation 1981-11-10 |