The following data is part of a premarket notification filed by Concept, Inc. with the FDA for C-cord.
| Device ID | K782046 |
| 510k Number | K782046 |
| Device Name: | C-CORD |
| Classification | Cord, Electric, For Endoscope |
| Applicant | CONCEPT, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FFZ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-12-08 |
| Decision Date | 1979-01-10 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() C-CORD 73211354 1158898 Dead/Cancelled |
CONCEPT, INC. 1979-04-12 |