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 |